Journal articles: 'Legh family'

1

Kurowska, Teresa. "Protection of the family farm – remarks of de lege lata and de lege ferenda character." Studia Iuridica Agraria 8 (2010): 14–29. http://dx.doi.org/10.15290/sia.2010.08.02.

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Boot, P., JAH Eekhof, and A. Knuistingh Neven. "Restless legs-syndroom." Huisarts en Wetenschap 46, no. 10 (October 2003): 323–26. http://dx.doi.org/10.1007/bf03083306.

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. "Restless legs-syndroom." Huisarts en Wetenschap 47, no. 1 (January 2004): 1015. http://dx.doi.org/10.1007/bf03084085.

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4

Verheij, Theo. "De huisarts staat niet met lege handen." Huisarts en Wetenschap 51, no. 4 (April 2008): 166. http://dx.doi.org/10.1007/bf03086717.

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Ohtsuka, Susumu, Dhugal J. Lindsay, and Kunihiko Izawa. "A new genus and species of the family Pennellidae (Copepoda, Siphonostomatoida) infecting the Pacific viperfish Chauliodus macouni." Parasite 25 (2018): 6. http://dx.doi.org/10.1051/parasite/2018003.

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A new genus and species of pennellid copepod, Protosarcotretes nishikawai n. g., n. sp., is described on the basis of an ovigerous female infecting a Pacific viperfish Chauliodus macouni collected from the deep-waters of Suruga Bay, Japan. The new genus exhibits the most plesiomorphic states in the first to fourth legs of pennellids, and is differentiated from two closely related pennellid genera Sarcotretes and Lernaeenicus by the morphology of the oral appendages. Two species of the genus Lernaeenicus are transferred to the new genus as Protosarcotretes multilobatus (Lewis, 1959) n. comb. and Protosarcotretes gnavus (Leigh-Sharpe, 1934) n. comb. The host specificity and life cycle of deep-sea pennellids are discussed. Sarcotretes scopeli Jungersen, 1911 and Cardiodectes bellottii (Richiardi, 1882) show low differentiated host-specificity, while P. nishikawai seems to be limited to the Stomiidae, which are rare hosts of pennellids, in contrast to the Myctophidae family. In the Pennellidae family, two patterns of the life cycle are found: with or without naupliar stages.

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Sugita, Yasuyuki. "Is restless legs syndrome an entirely neurological disorder?" European Journal of General Practice 14, no. 1 (January 2008): 45–46. http://dx.doi.org/10.1080/13814780802095550.

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7

Lucassen, Peter. "IJzer of geen ijzer bij het restless-legs syndrome." Huisarts en wetenschap 62, no. 9 (August 21, 2019): 63. http://dx.doi.org/10.1007/s12445-019-0227-3.

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8

Happe, Svenja, Sylvia Kotterba, Anna Heidbreder, Ulf Kallweit, Geert Mayer, Heike Benes, and Magdolna Hornyak. "Begutachtung des Restless-legs-Syndroms." Nervenheilkunde 40, no. 07 (June 2021): 550–57. http://dx.doi.org/10.1055/a-1389-6954.

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ZUSAMMENFASSUNGDas Restless-legs-Syndrom (RLS) ist eine der häufigsten neurologischen Erkrankungen. Gutachterliche Fragestellungen bei RLS-Patienten nehmen seit den vergangenen Jahren stetig zu. Daher hat die AG Motorik und Schlaf der Deutschen Gesellschaft für Schlafforschung und Schlafmedizin (DGSM) 2006 erstmals Empfehlungen zur Begutachtung und sozialmedizinischen Einschätzung des RLS erarbeitet. Im Folgenden werden die spezifischen Empfehlungen zur Beurteilung des RLS im Rahmen gutachterlicher Verfahren in einer Neubearbeitung vorgestellt. Diese Empfehlungen stellen eine Grundlage zur Vereinheitlichung und Qualitätssicherung in der Begutachtung des RLS dar, sie sollen jedoch nicht in die individuelle Freiheit und Verantwortung des jeweils beauftragten Gutachters eingreifen. Da bisher keine evidenzbasierten Studien über das RLS vorliegen, die die Besonderheiten der gutachterlichen Situation berücksichtigen, sind diese Empfehlungen als Konsensusdokument konzipiert.

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. "Leg altijd morfinepompje aan bij terminale sedatie." Huisarts en Wetenschap 52, no. 1 (January 2009): 54. http://dx.doi.org/10.1007/bf03085502.

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10

Stockton, Elizabeth. "Family, Kinship, and Sympathy in Nineteenth-Century American Literature (review)." Legacy 23, no. 1 (2006): 94–95. http://dx.doi.org/10.1353/leg.2006.0013.

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Protsailo, M. D., and I. O. Kryckyy. "Family case of Legg-Calve-Perthes disease." Paediatric Surgery. Ukraine, no. 2(63) (June 30, 2019): 104–8. http://dx.doi.org/10.15574/ps.2019.63.104.

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O??SULLIVAN, M., S. K. O??ROURKE, and P. MACAULEY. "Legg-Calv??-Perthes Disease in a Family." Clinical Orthopaedics and Related Research &NA;, no. 199 (October 1985): 179???181. http://dx.doi.org/10.1097/00003086-198510000-00024.

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13

O’Flynn, Norma, Mark Vaughan, and Kate Kelley. "Diagnosis and management of varicose veins in the legs: NICE guideline." British Journal of General Practice 64, no. 623 (May 27, 2014): 314–15. http://dx.doi.org/10.3399/bjgp14x680329.

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14

Baker, W. L., C. M. White, and C. I. Coleman. "Effect of Nonergot Dopamine Agonists on Symptoms of Restless Legs Syndrome." Annals of Family Medicine 6, no. 3 (May 1, 2008): 253–62. http://dx.doi.org/10.1370/afm.845.

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15

Allen, R. P., M. C. La Buda, P. Becker, and C. J. Earley. "Family history study of the restless legs syndrome." Sleep Medicine 3 (November 2002): S3—S7. http://dx.doi.org/10.1016/s1389-9457(02)00140-5.

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16

Peter, Natalie. "Family Foundations in Switzerland." Trusts & Trustees 26, no. 6 (July 1, 2020): 580–89. http://dx.doi.org/10.1093/tandt/ttaa049.

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Abstract At a governmental level, the introduction of a Swiss law on trusts is currently being reviewed. One of the arguments is that Switzerland does not provide for a suitable instrument to be used for estate planning or asset protection purposes. Many scholars and practitioners take the view, though, that a common law trust is not a suitable instrument and that therefore it would be more advisable to review the existing instruments, such as the Swiss family foundation or the fiducie (Treuhand), and to amend them accordingly. This article shall shed some light on the Swiss family foundation, on its use and limits and how it could be used de lege ferenda in the future if its legal limits were finally to be released.

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17

Gallardo, Jaime, Ramón Rodríguez, Martín Caudillo, and José M. Rico. "A family of spherical parallel manipulators with two legs." Mechanism and Machine Theory 43, no. 2 (February 2008): 201–16. http://dx.doi.org/10.1016/j.mechmachtheory.2007.02.001.

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18

Pennisi, Elizabeth. "Was Lucy's a Fighting Family? Look at Her Legs." Science 311, no. 5759 (January 20, 2006): 330.2–330. http://dx.doi.org/10.1126/science.311.5759.330b.

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19

Weissbach, Anne, Katharina Siegesmund, Norbert Brüggemann, Alexander Schmidt, Meike Kasten, Irene Pichler, Hiltrud Muhle, et al. "Exome sequencing in a family with restless legs syndrome." Movement Disorders 27, no. 13 (November 2012): 1686–89. http://dx.doi.org/10.1002/mds.25191.

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20

D'Avino, P. P., and C. S. Thummel. "crooked legs encodes a family of zinc finger proteins required for leg morphogenesis and ecdysone-regulated gene expression during Drosophila metamorphosis." Development 125, no. 9 (May 1, 1998): 1733–45. http://dx.doi.org/10.1242/dev.125.9.1733.

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Drosophila imaginal discs undergo extensive pattern formation during larval development, resulting in each cell acquiring a specific adult fate. The final manifestation of this pattern into adult structures is dependent on pulses of the steroid hormone ecdysone during metamorphosis, which trigger disc eversion, elongation and differentiation. We have defined genetic criteria that allow us to screen for ecdysone-inducible regulatory genes that are required for this transformation from patterned disc to adult structure. We describe here the first genetic locus isolated using these criteria: crooked legs (crol). crol mutants die during pupal development with defects in adult head eversion and leg morphogenesis. The crol gene is induced by ecdysone during the onset of metamorphosis and encodes at least three protein isoforms that contain 12–18 C2H2 zinc fingers. Consistent with this sequence motif, crol mutations have stage-specific effects on ecdysone-regulated gene expression. The EcR ecdysone receptor, and the BR-C, E74 and E75 early regulatory genes, are submaximally induced in crol mutants in response to the prepupal ecdysone pulse. These changes in gene activity are consistent with the crol lethal phenotypes and provide a basis for understanding the molecular mechanisms of crol action. The genetic criteria described here provide a new direction for identifying regulators of adult tissue development during insect metamorphosis.

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21

Kotterba, Sylvia. "Parasomnien." Nervenheilkunde 40, no. 07 (June 2021): 540–44. http://dx.doi.org/10.1055/a-1469-7734.

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ZUSAMMENFASSUNGBewegungen im Schlaf sind prinzipiell physiologisch. In der Internationalen Klassifikation von Schlafstörungen (ICSD 3) werden Bewegungen (insbesondere das Restless-legs-Syndrom) und Parasomnien aufgeführt, die durch Beeinträchtigung des Betroffenen einer Abklärung und ggf. auch einer Therapie bedürfen. Bewegungen im Rahmen von Parasomnien können zu Verletzungen der Betroffenen und der Bettpartner führen, sexuelle Übergriffe sind möglich. Dieser Artikel soll einen Überblick über die Diagnostik und ggf. forensische Bedeutung von Parasomnien geben. Insbesondere soll auf die möglichen Therapien bzw. Vorsorgemechanismen eingegangen werden.

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22

LIN, YUCHENG. "First report of the spider genus Symphytognatha from Asia (Araneae, Symphytognathidae)." Zootaxa 4638, no. 2 (July 16, 2019): 291–95. http://dx.doi.org/10.11646/zootaxa.4638.2.8.

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Symphytognatha Hickman, 1931 was originally erected by Hickman (1931) as the type genus of the spider family Symphytognathidae. Forster and Platnick (1977) reviewed the family and proposed a diagnosis for Symphytognatha: almost completely fused chelicerae with a visible suture line and multidentate superior claws on legs I and II (but not on legs III and IV). Currently this genus contains 14 species (World Spider Catalog 2019), mainly widespread in South Africa (Griswold 1987), Oceania (Hickman 1931, Forster & Platnick 1977, Platnick 1979, Harvey 1992, 2001), and Central and South America (Balogh & Loksa 1968, Forster & Platnick 1977, Georgescu 1988, Brescovit, Álvares & Lopes 2004, Dupérré & Tapia 2017).

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23

Bates, Katharine Lee. "For Katharine Coman's Family and Innermost Circle of Friends. Not for Print nor in any way for General Circulation." Legacy 23, no. 1 (2006): 74–85. http://dx.doi.org/10.1353/leg.2006.0002.

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24

Symvoulakis, Emmanouil, Dimitrios Anyfantakis, and Christos Lionis. "Restless legs syndrome: literature review." Sao Paulo Medical Journal 128, no. 3 (May 2010): 167–70. http://dx.doi.org/10.1590/s1516-31802010000300008.

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Restless legs syndrome is a distressing condition, with negative effects on sleep and daytime activities that affect personal, family and occupational life. The overall impact of restless legs syndrome on quality of life is comparable to that of chronic and frustrating conditions such as depression and diabetes. Misdiagnosis and inappropriate treatment may increase patients' suffering in terms of uncertainty, overuse or misuse of care services and lack of trust. Presenting a synthesis of the main topics in the literature on restless legs syndrome facilitates for a better understanding and its management in primary care settings.

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25

Kenkre, JE, FDR Hobbs, YH Carter, RL Holder, and EP Holmes. "A randomized controlled trial of electromagnetic therapy in the primary care management of venous leg ulceration." Family Practice 13, no. 3 (1996): 236–41. http://dx.doi.org/10.1093/fampra/13.3.236.

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26

Mkaouar-Rebai, Emna, Wissem Chaari, Samia Younes, Raoudha Bousoffara, Mohamed Tahar Sfar, and Faiza Fakhfakh. "Maternally Inherited Leigh Syndrome: T8993G Mutation in a Tunisian Family." Pediatric Neurology 40, no. 6 (June 2009): 437–42. http://dx.doi.org/10.1016/j.pediatrneurol.2009.01.004.

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27

Pizza, F., E. Persici, G. La Manna, C. Campieri, G. Plazzi, E. Carretta, M. L. Cappuccilli, B. Ferri, S. Stefoni, and P. Montagna. "Family recurrence and oligo-anuria predict uremic restless legs syndrome." Acta Neurologica Scandinavica 125, no. 6 (August 9, 2011): 403–9. http://dx.doi.org/10.1111/j.1600-0404.2011.01581.x.

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28

Currie, J. "Commentary: Will the 'Long Arm of the Family' have legs?" International Journal of Epidemiology 38, no. 3 (April 6, 2009): 744–45. http://dx.doi.org/10.1093/ije/dyp154.

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29

Alfadhel, Majid. "Early Infantile Leigh-like SLC19A3 Gene Defects Have a Poor Prognosis: Report and Review." Journal of Central Nervous System Disease 9 (January 1, 2017): 117957351773752. http://dx.doi.org/10.1177/1179573517737521.

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Solute carrier family 19 (thiamine transporter), member 3 ( SCL19A3) gene defect produces an autosomal recessive neurodegenerative disorder associated with different phenotypes and acronyms. One of the common presentations is early infantile lethal Leigh-like syndrome. We report a case of early infantile Leigh-like SLC19A3 gene defects of patients who died at 4 months of age with no response to a high dose of biotin and thiamine. In addition, we report a novel mutation that was not reported previously. Finally, we review the literature regarding early infantile Leigh-like SLC19A3 gene defects and compare the literature with our patient.

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30

Mortensen, Ole Hartvig, Peter Plomgaard, Christian P. Fischer, Anne K. Hansen, Henriette Pilegaard, and Bente Klarlund Pedersen. "PGC-1β is downregulated by training in human skeletal muscle: no effect of training twice every second day vs. once daily on expression of the PGC-1 family." Journal of Applied Physiology 103, no. 5 (November 2007): 1536–42. http://dx.doi.org/10.1152/japplphysiol.00575.2007.

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We hypothesized that the peroxisome proliferator-activated receptor-γ coactivator-1 (PGC-1) family of transcriptional coactivators (PGC-1α, PGC-1β, and PRC) is differentially regulated by training once daily vs. training twice daily every second day and that this difference might be observed in the acute response to endurance exercise. Furthermore, we hypothesized that expression levels of the PGC-1 family differ with muscular fiber-type composition. Thus, before and after 10 wk of knee extensor endurance training, training one leg once daily and the other leg twice daily every second day, keeping the total amount of training for the legs equal, skeletal muscle mRNA expression levels of PGC-1α, PGC-1β, and PRC were determined in young healthy men ( n = 7) in response to 3 h of acute exercise. No significant difference was found between the two legs, suggesting that regulation of the PGC-1 family is independent of training protocol. Training decreased PGC-1β in both legs, whereas PGC-1α was increased, but not significantly, in the leg training once daily. PRC did not change with training. Both PGC-1α and PRC were increased by acute exercise both before and after endurance training, whereas PGC-1β did not change. The mRNA levels of the PGC-1 family were examined in different types of human skeletal muscle (triceps, soleus, and vastus lateralis; n = 7). Only the expression level of PGC-1β differed and correlated inversely with percentage of type I fibers. In conclusion, there was no difference between training protocols on the acute exercise and training response of the PGC-1 family. However, training caused a decrease in PGC-1β mRNA levels.

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31

Di Gregorio, Raffaele. "Analytic Form Solution of the Direct Position Analysis of a Wide Family of Three-Legged Parallel Manipulators." Journal of Mechanical Design 128, no. 1 (January 17, 2005): 264–71. http://dx.doi.org/10.1115/1.1913703.

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A wide family of parallel manipulators (PMs) is the one that groups all PMs with three legs where the legs become kinematic chains constituted of a passive spherical pair (S) in series with either a passive prismatic pair (P) or a passive revolute pair (R) when the actuators are locked. The topologies of the structures generated by these manipulators, when the actuators are locked, are ten. Two out of these topologies are the SR-2PS topology (one SR leg and two PS legs) and the SP-2RS topology (one SP leg and two RS legs). This paper presents two algorithms. The first one determines all the assembly modes of the SR-2PS structures. The second one determines all the assembly modes of the SP-2RS structures. The presented algorithms can be applied without changes to solve, in analytical form, the direct position analysis (DPA) of all the parallel manipulators that generate a SR-2PS structure or a SP-2RS structure when the actuators are locked. In particular, the closure equations of two generic structures, one of type SR-2PS and the other of type SP-2RS, are written. The eliminants of the two systems of equations are determined and the solution procedures are presented. Finally, the proposed procedures are applied to real cases. This work demonstrates that (i) the DPA solutions of any PM that becomes a SR-2PS structure are at most eight, and (ii) the DPA solutions of any PM that becomes a SP-2RS structure are at most sixteen.

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32

Miró, Òscar. "Elementos para mejorar la difusión de la reanimación cardiopulmonar entre la población lega." Atención Primaria 45, no. 10 (December 2013): 544–45. http://dx.doi.org/10.1016/j.aprim.2013.04.008.

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33

Spießhöfer, Jens, Peter Young, and Matthias Boentert. "Neuromuskuläre Erkrankungen und Schlaf." Nervenheilkunde 38, no. 03 (February 2019): 108–14. http://dx.doi.org/10.1055/a-0818-9117.

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ZusammenfassungViele neuromuskuläre Erkrankungen (NME) sind mit Begleitsymptomen verbunden, die den Schlaf und die Schlafqualität beeinträchtigen. Schlafstörungen können eine unspezifische Folge der Immobilisierung darstellen, aber besonders bei Erkrankungen des peripheren Nervensystems auch auf nächtliche Crampi oder ein Restless-legs-Syndrom zurückzuführen sein. Motoneuronerkrankungen, akute Immunneuropathien und viele Myopathien können im Verlauf mit einer relevanten Schwäche der Atemmuskulatur einhergehen, die sich initial als schlafbezogene Hypoventilation manifestiert und bis zur hyperkapnischen respiratorischen Insuffizienz voranschreiten kann. Zahlreiche Erkrankungen sind zudem mit einem erhöhten Risiko für eine obstruktive Schlafapnoe assoziiert. Schlafbezogene Symptome sind bei NME häufig und sollten gezielt erfragt werden, um eine geeignete Diagnostik und Therapie zu ermöglichen.

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34

OConnor, Barry M. "BOCHKOVOCOPTIDAE, AN UNUSUAL NEW FAMILY OF PSOROPTIDIAN MITES (ACARI: ASTIGMATA) ASSOCIATED WITH OTOMYS DENTI (RODENTIA: MURIDAE) FROM UGANDA." Acarina 27, no. 2 (December 30, 2019): 145–50. http://dx.doi.org/10.21684/0132-8077-2019-27-2-145-150.

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A new family, Bochkovocoptidae, is proposed for a new genus and species of psoroptidian mite (Astigmata), Bochkovocoptes otomys sp. n., collected from the follicles of the facial vibrissae of Otomys denti (Rodentia: Muridae) from Uganda. The new taxon is characterized by retrorse processes and striated apical membranes on the subcapitular rutella, strong retrorse processes on the segments of the anterior legs, well developed pretarsi on legs I–III and a reduced pretarsus on leg IV. The new taxon is hypothesized to be related to the families Sarcoptidae and Rhyncoptidae.

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35

ROTHERY, MARK, and JON STOBART. "Inheritance events and spending patterns in the English country house: the Leigh family of Stoneleigh Abbey, 1738–1806." Continuity and Change 27, no. 3 (December 2012): 379–407. http://dx.doi.org/10.1017/s0268416012000203.

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This article analyses the everyday spending patterns of the Leigh family of Stoneleigh Abbey, Warwickshire, in relation to inheritance, demography and trusteeship. The analysis makes use of a large dataset of receipted bills along with various other types of accounts and legal documents. We show that several factors contributed to the survival and flourishing of the Leigh estates. These included: first, moderate levels of spending by successive owners of the family estates, punctuated by periodic surges in spending following inheritance events; second, demographic factors; and, third, the responsible management of the estate by trustees during periods of minority. This analysis illustrates that careful economic management, rather than conspicuous consumption, was the defining feature of wealthy landed families such as the Leighs.

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Delacour, Chloé, Juliette Chambe, François Lefebvre, Claire Bodot, Elodie Bigerel, Laetitia Epifani, Céline Granda, Dagmar M. Haller, and Hubert Maisonneuve. "Association Between Alcohol Consumption and Nocturnal Leg Cramps in Patients Over 60 Years Old: A Case-Control Study." Annals of Family Medicine 16, no. 4 (July 2018): 296–301. http://dx.doi.org/10.1370/afm.2238.

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37

Crocombe, Dominic, and Mayukh Bhattacharyya. "Non-traumatic cervical disc prolapse with spinal cord compression: an unlikely but important cause of leg and back pain." British Journal of General Practice 68, no. 671 (May 31, 2018): 296–97. http://dx.doi.org/10.3399/bjgp18x696581.

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38

Mumoli, Nicola, Josè Vitale, Matteo Giorgi-Pierfranceschi, Silvia Sabatini, Renato Tulino, Marco Cei, Eugenio Bucherini, et al. "General Practitioner–Performed Compression Ultrasonography for Diagnosis of Deep Vein Thrombosis of the Leg: A Multicenter, Prospective Cohort Study." Annals of Family Medicine 15, no. 6 (November 2017): 535–39. http://dx.doi.org/10.1370/afm.2109.

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39

Watzke, Stefan, and Peter Brieger. "Neuropsychologische Prädiktoren für den Erfolg beruflicher Wiedereingliederung." Nervenheilkunde 38, no. 07 (July 2019): 474–80. http://dx.doi.org/10.1055/a-0888-4926.

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ZUSAMMENFASSUNGKognitive Leistungseinschränkungen stellen zentrale Erkrankungsmerkmale der Schizophrenie und wichtige Prognosefaktoren für den funktionalen Outcome Betroffener dar. In der beruflichen Rehabilitation werden sie daher als Zielgrößen für Trainings einerseits und als Erfolgsprädiktoren andererseits genutzt. Bei zunehmender Diversifizierung der rehabilitativen Angebote und der angesprochenen Klientel stellt sich die Frage, ob kognitive Defizite zielgruppen- und maßnahmenübergreifend ihre wichtige Funktion beibehalten können.Eine Durchsicht der Literatur legt nahe, dass die zentralen Aussagen zu prognostischer Validität und Adressierbarkeit mittels kognitiver Trainings auf Patienten mit affektiven Störungen grundsätzlich ausgeweitet werden kann. Für Rehabilitanden anderer diagnostischer Gruppen liegen kaum Studien zur Erfolgsprognose vor. Es muss aber davon ausgegangen werden, dass bei nur geringen kognitiven Beeinträchtigungen andere Merkmale – z. B. Angst, Metakognitionen und Fähigkeiten der sozialen Kognition – zur Prognoseabschätzung herangezogen werden müssen.

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40

Harvey, MS. "Pezidae, a new freshwater mite family from Australia (Acarina : Halacaroidea)." Invertebrate Systematics 3, no. 6 (1989): 771. http://dx.doi.org/10.1071/it9890771.

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A new halacaroid family, Pezidae, is erected for the new genus Peza, with two new species Peza ops (type species) and Peza daps. P. ops has been widely collected in south-eastern Australia, while P. daps is known only from a single female taken from the gill chamber of a burrowing crayfish, Engaeus fultoni Smith & Schuster (Crustacea : Decapoda : Parastacidae), in the Otway Ranges, Victoria. During winter and spring, females of both species apparently attach their eggs to their hind legs. The Pezidae is regarded as the sister-group of the remaining Halacaroidea.

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41

Puślecki, Damian. "Problems of Legal Definition of Family Farm in Poland." EU agrarian Law 5, no. 2 (December 1, 2016): 20–24. http://dx.doi.org/10.1515/eual-2016-0008.

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Abstract The paper discusses the issues relating to the legal definition of the family farm as the foundation of the agricultural system in Poland. According to Article 23 of the Constitution of 1997, the family farm is the basis of the Polish agricultural system. By means of analysing the provisions of the Constitution and the Act on the Agricultural System, the paper points out current tendencies in the Polish agricultural system. The main aim of this article is to identify individual elements of the legal definition of the family farm and to evaluate already existing solutions on the matter. The final part of the paper presents de lege ferenda postulates.

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42

Puschmann, A., R. F. Pfeiffer, A. J. Stoessl, R. Kuriakose, J. L. Lash, J. A. Searcy, A. J. Strongosky, et al. "A family with parkinsonism, essential tremor, restless legs syndrome, and depression." Neurology 76, no. 19 (May 9, 2011): 1623–30. http://dx.doi.org/10.1212/wnl.0b013e318219fb42.

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43

Chakrapani, A., L. Heptinstall, and J. Walter. "A family with Leigh syndrome caused by the rarer T8993C mutation." Journal of Inherited Metabolic Disease 21, no. 6 (August 1998): 685–86. http://dx.doi.org/10.1023/a:1005401121344.

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44

Sebo, P., B. Cerutti, and D. M. Haller. "Effect of magnesium therapy on nocturnal leg cramps: a systematic review of randomized controlled trials with meta-analysis using simulations." Family Practice 31, no. 1 (November 26, 2013): 7–19. http://dx.doi.org/10.1093/fampra/cmt065.

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Kolářová, L., K. Skirnisson, and P. Horák. "Schistosome cercariae as the causative agent of swimmer's itch in Iceland." Journal of Helminthology 73, no. 3 (March 1999): 215–20. http://dx.doi.org/10.1017/s0022149x99000335.

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During late summer in 1995 to 1997, repeated outbreaks of maculopapular skin eruptions were noted on the legs of children after wading in the pond in the Family Park in Laugardalur, Reykjavík, Iceland. Clinical symptoms developing on the legs resembled those of cercarial dermatitis. An examination ofLymnaea peregrasnails from this pond and from the adjacent Lake Tjornin resulted in detection of previously undescribed schistosome cercariae. This is the first report of schistosomes in Iceland and also the most northern occurrence of these parasites in Europe.

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PLATNICK, NORMAN I. "Reification, Matrices, and the Interrelationships of Goblin Spiders." Zootaxa 3608, no. 4 (January 21, 2013): 278–80. http://dx.doi.org/10.11646/zootaxa.3608.4.6.

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In a recent review of the interrelationships of goblin spiders (the family Oonopidae), Platnick et al. (2012) presented a new subfamily-level classification of the family, replacing older arrangements that included at least one paraphyletic group. That analysis was based heavily on new evidence obtained, by an international consortium of researchers, through scanning electron microscopy of the tarsal organs, tiny chemoreceptors found near the tips of the legs and pedipalps.

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Chatterton, Chris, Andrew Ross, and Wilfried Wichard. "Corydasialidae fam. n. (Megaloptera) from Baltic amber." Insect Systematics & Evolution 36, no. 3 (2005): 279–84. http://dx.doi.org/10.1163/187631205788838410.

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AbstractA new family of the order Megaloptera from Baltic amber is suggested: Corydasialidae fam. n. The type species is Corydasialis inexspectatus gen. & sp. n. The new family is characterized by some autapomorphic traits: 4th tarsal segments of the legs are bilobed, underside of the 4th tarsal lobes with a brush of sucker disc-shaped hairs, in forewings Sc and R1 are not fused and both CuA and CuP distinctly forked.

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Chursina, Mariya Alexandrovna, and Oleg Pavlovich Negrobov. "Legs morphometric characters of the Dolichopus Latreille species, 1796 (Diptera, Dolichopodidae)." Samara Journal of Science 9, no. 1 (February 28, 2020): 106–12. http://dx.doi.org/10.17816/snv202091117.

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A comparative analysis of 30 species of the Dolichopodidae family in a phylogenetic context was conducted to examine interspecific variation in the legs morphometry. Five relative traits of legs from 12 and seven absolute traits from nine showed significant phylogenetic signal. A set of traits, such as relatively short hind tibia and relatively long fore and middle tibia and the first segments of the hind legs allowed to allocate Dolichopus species from the other ones. The projection of the phylogenetic tree of Dolichopus species into the morphospace allowed us to divide it into four individual areas: not closely related species, but species having similar modifications of males legs tended to cluster. This suggests that the legs morphometric traits should be mainly under pressure of sexual selection. It has also been revealed that the elongation of the first segment of hind tarsi in Dolichopus species is associated with the distal displacement of the insertion point of dm-m with M4 and the decrease of the length of R4+5 . The functional significance of these characters set is discussed.

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Pontifex, CS, LE Hamilton, K. Martens, and G. Pfeffer. "P.074 Clinical features of a family with distal myopathy and rimmed vacuoles due to a digenic interaction." Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques 45, s2 (June 2018): S35. http://dx.doi.org/10.1017/cjn.2018.176.

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Background: The interaction between mutations in two or more genes is increasingly recognised as an important contributor to the phenotypic variability in genetic disorders. Co-occurrence of variants in SQSTM1 and TIA1 is reported as a cause of myopathy in 3 prior cases, but limited clinical data were presented. We present detailed clinical features of a family with two siblings having a distal myopathy with rimmed vacuoles (DMRV), and genetic variants in SQSTM1 and TIA1. Methods: Clinicopathologic study of a family with DMRV to describe clinical features, laboratory and neurophysiology studies, neuroimaging, and genetic sequencing. Results: Two siblings with variants in SQSTM1 and TIA1 developed myopathy in their early 60’s, with early involvement of ankle dorsiflexors and finger extensors. A decade after onset, patients remain ambulatory and have not developed cardiac or respiratory complications. MRI of the legs showed selective involvement of adductor magnus, vastus lateralis, and in lower legs the anterior compartment and medial gastrocnemius. Muscle pathology demonstrated rimmed vacuoles, disrupted myofibrillar architecture, and mislocalised TDP43. Two unaffected family members had one genetic variant but not both. Conclusions: We describe a fourth family with co-occurrence of TIA1 and SQSTM1 genetic variants and describe their detailed phenotype. Future study should address the mechanism of the interaction between these two variants.

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Alexander, Samuel Allen. "Intelligence via ultrafilters: structural properties of some intelligence comparators of deterministic Legg-Hutter agents." Journal of Artificial General Intelligence 10, no. 1 (January 1, 2019): 24–45. http://dx.doi.org/10.2478/jagi-2019-0003.

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Abstract Legg and Hutter, as well as subsequent authors, considered intelligent agents through the lens of interaction with reward-giving environments, attempting to assign numeric intelligence measures to such agents, with the guiding principle that a more intelligent agent should gain higher rewards from environments in some aggregate sense. In this paper, we consider a related question: rather than measure numeric intelligence of one Legg-Hutter agent, how can we compare the relative intelligence of two Legg-Hutter agents? We propose an elegant answer based on the following insight: we can view Legg-Hutter agents as candidates in an election, whose voters are environments, letting each environment vote (via its rewards) which agent (if either) is more intelligent. This leads to an abstract family of comparators simple enough that we can prove some structural theorems about them. It is an open question whether these structural theorems apply to more practical intelligence measures.

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Journal articles on the topic 'Legh family'

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