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Journal articles on the topic 'Soulier'

Author: Grafiati

Published: 13 April 2024

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1

Shitikova, A. S., Z. D. Fedorova, O. E. Belyazo, et al. "Bernard-Soulier disease." Kazan medical journal 68, no. 2 (1987): 124–30. http://dx.doi.org/10.17816/kazmj96033.

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Bernard-Soulier disease, a congenital macrocytic thrombocytopathy, was first described in 1948. Currently, this pathology has again attracted the attention of many researchers, as the study of its pathogenesis has deepened the understanding of the mechanisms of the hemostatic process concerning the interaction of platelets with the damaged vessel wall. This rare disease (70 cases were described by 1983) is inherited as an incomplete autosomal recessive trait and is observed with equal frequency in males and females. Bleeding from mucous membranes of the nose, mouth and other organs, petechiae

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2

Berndt, M. C., and R. K. Andrews. "Bernard-Soulier syndrome." Haematologica 96, no. 3 (2011): 355–59. http://dx.doi.org/10.3324/haematol.2010.039883.

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3

López, José A., Robert K. Andrews, Vahid Afshar-Kharghan, and Michael C. Berndt. "Bernard-Soulier Syndrome." Blood 91, no. 12 (1998): 4397–418. http://dx.doi.org/10.1182/blood.v91.12.4397.

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4

López, José A., Robert K. Andrews, Vahid Afshar-Kharghan, and Michael C. Berndt. "Bernard-Soulier Syndrome." Blood 91, no. 12 (1998): 4397–418. http://dx.doi.org/10.1182/blood.v91.12.4397.412k42_4397_4418.

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5

MENACHE, D. "Jean-Pierre Soulier." Revue Francaise de Transfusion et Immuno-hématologie 28, no. 6 (1985): 565–70. http://dx.doi.org/10.1016/s0338-4535(85)80001-5.

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6

SOULIER-PERKINS, ADELINE, and GERNOT KUNZ. "Revision of the malagassy endemic genus Amberana Distant (Hemiptera, Cercopidae) with description of one new genus." Zootaxa 3156, no. 1 (2012): 1. http://dx.doi.org/10.11646/zootaxa.3156.1.1.

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The genus Amberana Distant is revised. Three new species, A. attei Soulier-Perkins sp. n., A. ouvrardi Soulier-Perkinssp. n. and A. pascali Soulier-Perkins sp. n. are described. Lectotypes are designated for A. dimidiata (Signoret, 1960), A.fissurata Jacobi, 1917, A. noualhieri (Lallemand, 1920), A. sexguttata (Melichar, 1915) and A. uncinata Jacobi, 1917. Am-berana tripunctata var. completa Lallemand, 1949 and A. tripunctata Lallemand, 1920 are synonymised with A. bergevini(Lallemand, 1920). A new genus, Bourgoinrana Soulier-Perkins gen. n., is erected for B. perinetana (Synave, 1957),comb. n

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7

Louguet, Claire. "Philippe Soulier, Simplicius et." Philosophie antique, no. 15 (November 24, 2015): 291–94. http://dx.doi.org/10.4000/philosant.482.

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8

Desplanque, Gilles. "Ambleny (Aisne). Le Soulier." Archéologie médiévale, no. 42 (December 1, 2012): 176. http://dx.doi.org/10.4000/archeomed.10739.

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9

Galmiche, Thierry. "Ambleny (Aisne). Le Soulier." Archéologie médiévale, no. 41 (December 1, 2011): 183. http://dx.doi.org/10.4000/archeomed.11515.

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10

Rouger, P. "Professor Jean Pierre Soulier." Vox Sanguinis 84, no. 3 (2003): 163. http://dx.doi.org/10.1046/j.1423-0410.2003.00309.x.

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11

Konkle, Barbara A. "The Bernard-Soulier Syndrome." Trends in Cardiovascular Medicine 7, no. 7 (1997): 239–44. http://dx.doi.org/10.1016/s1050-1738(97)00064-9.

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12

Lefrère, J. J. "Jean-Pierre Soulier écrivain." Transfusion Clinique et Biologique 11, no. 1 (2004): 71–73. http://dx.doi.org/10.1016/j.tracli.2003.12.004.

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13

Berndt, Michael C., Dominique J. Fournier, and Peter A. Castaldi. "4 Bernard-Soulier syndrome." Baillière's Clinical Haematology 2, no. 3 (1989): 585–607. http://dx.doi.org/10.1016/s0950-3536(89)80035-6.

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14

Hahn, Thomas. "noé soulier «first memory»." tanz 14, no. 1 (2023): 37. http://dx.doi.org/10.5771/1869-7720-2023-1-037.

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15

Berthier, Philippe. "Sous le soulier de Satan." Roman 20-50 54, no. 2 (2012): 99. http://dx.doi.org/10.3917/r2050.054.0099.

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16

Neuweiler, W., and Alice Hess. "Bestimmung der Prothrombinzeit nach Soulier." DMW - Deutsche Medizinische Wochenschrift 75, no. 06 (2009): 196–99. http://dx.doi.org/10.1055/s-0028-1117827.

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17

Muller, J. Y. "Jean-Pierre Soulier (1915–2003)." Transfusion Clinique et Biologique 11, no. 1 (2004): 57–64. http://dx.doi.org/10.1016/j.tracli.2003.11.005.

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18

Mant, Michael J. "DDAVP in Bernard-Soulier syndrome." Thrombosis Research 52, no. 1 (1988): 77–78. http://dx.doi.org/10.1016/0049-3848(88)90045-x.

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19

PRABU, P., and L. A. PARAPIA. "Bernard-Soulier syndrome in pregnancy." Clinical and Laboratory Haematology 28, no. 3 (2006): 198–201. http://dx.doi.org/10.1111/j.1365-2257.2006.00780.x.

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20

Andrews, Robert, and Michael Berndt. "Bernard-Soulier Syndrome: An Update." Seminars in Thrombosis and Hemostasis 39, no. 06 (2013): 656–62. http://dx.doi.org/10.1055/s-0033-1353390.

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21

Menache-Aronson, D. "Jean-Pierre Soulier, 1915-2003." Journal of Thrombosis and Haemostasis 1, no. 5 (2003): 1125–26. http://dx.doi.org/10.1046/j.1538-7836.2003.00258.x.

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22

Pires, João Victor Alcântara, Julliana Ferrari Campêlo Libório de Santana, Etienny de Brito Dias Fernandes, et al. "Tratamento cirúrgico de cisto ovariano roto em paciente com síndrome de Bernard-Soulier." Research, Society and Development 11, no. 2 (2022): e47911225366. http://dx.doi.org/10.33448/rsd-v11i2.25366.

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Introdução: A síndrome de Bernard-Soulier (SBS) é uma doença hematológica e hereditária rara que possui uma prevalência estimada em 1:1.000.000. Suas anormalidades são decorrentes da expressão defeituosa do complexo glicoproteico GPIb/IX/V- receptor plaquetário que é crucial para o estabelecimento da hemostasia primária. Objetivo: Relatar um caso raro de cisto ovariano roto em portador da Síndrome de Bernard-Soulier. Metodologia: estudo descritivo, transversal, que consiste na elaboração de um relato de caso, elaborado a partir de uma análise do prontuário de um paciente portador da Síndrome d

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23

Crispolon, Elorde Jr S., Eric Guilbert, Sheryl A. Yap, and Adeline Soulier-Perkins. "New genus and new species of spittlebugs (Hemiptera: Cercopidae) from the Philippines." European Journal of Taxonomy 778 (November 16, 2021): 90–135. http://dx.doi.org/10.5852/ejt.2021.778.1571.

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The following new taxa are described from the Philippines: Mioscarta nubisa Crispolon & Soulier-Perkins sp. nov., M. translucida Crispolon & Yap sp. nov. and Trigonoschema Crispolon & Soulier-Perkins gen. nov. with three new species: T. manoborum Crispolon & Soulier-Perkins sp. nov. (as type species), T. negrosensis Crispolon & Yap sp. nov and T. rubercella Crispolon & Guilbert sp. nov. Trigonoschema pallida (Lallemand, 1927) comb. nov. is transferred from Mioscarta Breddin, 1901. Descriptions of male genitalia are illustrated and keys to species of Philippine Mioscarta

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24

Devine, DV, MS Currie, WF Rosse, and CS Greenberg. "Pseudo-Bernard-Soulier syndrome: thrombocytopenia caused by autoantibody to platelet glycoprotein Ib." Blood 70, no. 2 (1987): 428–31. http://dx.doi.org/10.1182/blood.v70.2.428.428.

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Abstract The Bernard-Soulier syndrome is an inherited bleeding disorder that is due to a deficiency in platelet glycoprotein Ib. Bernard-Soulier platelets fail to agglutinate in response to ristocetin despite normal levels of factor VIII:von Willebrand factor. We report a patient who developed severe refractory thrombocytopenia postsurgically while receiving procainamide therapy. Thrombocytopenia was immune mediated since the patient's platelets bore high levels of antiplatelet antibody. Radioimmunoprecipitation studies demonstrated that the autoantibodies had specificity for platelet glycopro

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25

Devine, DV, MS Currie, WF Rosse, and CS Greenberg. "Pseudo-Bernard-Soulier syndrome: thrombocytopenia caused by autoantibody to platelet glycoprotein Ib." Blood 70, no. 2 (1987): 428–31. http://dx.doi.org/10.1182/blood.v70.2.428.bloodjournal702428.

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The Bernard-Soulier syndrome is an inherited bleeding disorder that is due to a deficiency in platelet glycoprotein Ib. Bernard-Soulier platelets fail to agglutinate in response to ristocetin despite normal levels of factor VIII:von Willebrand factor. We report a patient who developed severe refractory thrombocytopenia postsurgically while receiving procainamide therapy. Thrombocytopenia was immune mediated since the patient's platelets bore high levels of antiplatelet antibody. Radioimmunoprecipitation studies demonstrated that the autoantibodies had specificity for platelet glycoproteins Ib

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26

KUNISHIMA, Shinji. "Molecular Basis of Bernard-Soulier Syndrome." Japanese Journal of Thrombosis and Hemostasis 6, no. 2 (1995): 56–65. http://dx.doi.org/10.2491/jjsth.6.56.

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27

Hayashi, Tomohiro, and Keijiroh Suzuki. "Molecular Pathogenesis of Bernard-Soulier Syndrome." Seminars in Thrombosis and Hemostasis Volume 26, Number 01 (2000): 053–60. http://dx.doi.org/10.1055/s-2000-9804.

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28

Sandrock, Kirstin, Ralf Knöfler, Andreas Greinacher, et al. "Novel Mutation in Bernard-Soulier Syndrome." Transfusion Medicine and Hemotherapy 37, no. 5 (2010): 7. http://dx.doi.org/10.1159/000320255.

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29

Kunishima, Shinji, Tadashi Kamiya, and Hidehiko Saito. "Genetic Abnormalities of Bernard-Soulier Syndrome." International Journal of Hematology 76, no. 4 (2002): 319–27. http://dx.doi.org/10.1007/bf02982690.

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30

OKI, Yumiko, Kayo YOSHIOKA, Masato KONISHI, et al. "A case of Bernard-Soulier syndrome." Nihon Naika Gakkai Zasshi 76, no. 9 (1987): 1414–18. http://dx.doi.org/10.2169/naika.76.1414.

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31

Millet-Gérard, Dominique. "Beauté théologique du Soulier de Satin." Revue d'histoire littéraire de la France o 100, no. 6 (2000): 1547–58. http://dx.doi.org/10.3917/rhlf.g2000.100n6.1547.

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Résumé Les occurrences des mots «beau» et «beauté» dans Le Soulier de Satin sont étrangement conventionnelles.: il ne faut évidemment pas se laisser prendre à cette apparence, et le texte renferme aussi une réflexion, une méditation même sur le concept théologique du Beau, qui fait le lien entre nature et surnature ; aussi le terme de Beauté est-il relayé par l’imagerie lumineuse qui s’intensifie tout au long du drame, et concerne bien sûr aussi la mise en scène : c’est la splendeur de la Grâce qui doit ici être rendue, à travers une conception elle aussi très théolôgique — et baroque -— du th

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32

SOULIER-PERKINS, ADELINE, MARIO NAVASERO, SHERYL YAP, and MICHAEL R. WILSON. "New species for Virgilia Stål, 1870 (Hemiptera, Lophopidae), genus review and key to species." Zootaxa 4415, no. 1 (2018): 135. http://dx.doi.org/10.11646/zootaxa.4415.1.6.

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Two new species of the lophopid genus Virgilia Stål 1866, are described and illustrated, V. cocovora Soulier-Perkins sp. nov. and V. imuganensis Soulier-Perkins sp. nov. A key to the species of the genus is provided. Photos for the four Virgilia species are presented and the male terminalia illustrations are given. A comment on the potential pest status of one of the described species, V. cocovora, is given.

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33

Bouteille, Emilien, Maxime Le Cesne, and Adeline Soulier-Perkins. "Cercopidae spittle-bugs (Hemiptera, Cicadomorpha) of Madagascar: a new species of Bourgoinrana and revision of the Locris species." ZooKeys 1023 (March 10, 2021): 29–47. http://dx.doi.org/10.3897/zookeys.1023.58733.

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The Locris species and subspecies from Madagascar are revised and a new combination is proposed: Locris johannae var. nigrolimbata Lallemand, 1910 to L. nigrolimbatacomb. nov. Illustrations and description of male terminalia are given for the first time for the three Locris species and an identification key is provided. A new species of the Malagasy endemic genus Bourgoinrana Soulier-Perkins, 2012 is described: B. beondrokaensis Le Cesne &amp; Soulier-Perkins sp. nov. An updated identification key to the species of Bourgoinrana is provided.

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34

Drouin, J., JL McGregor, S. Parmentier, CA Izaguirre, and KJ Clemetson. "Residual amounts of glycoprotein Ib concomitant with near-absence of glycoprotein IX in platelets of Bernard-Soulier patients." Blood 72, no. 3 (1988): 1086–88. http://dx.doi.org/10.1182/blood.v72.3.1086.1086.

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Abstract A study of the Bernard-Soulier syndrome in two unrelated families using different polyclonal antibodies in a sensitive immunoblot assay showed residual amounts of platelet membrane glycoprotein (GP) lb in the eight homozygotes, as well as the near-absence of GPlb beta and GPIX. The eight heterozygotes studied showed a double band pattern for GPlb and about half the normal level of GPlb beta and GPIX. Therefore, we conclude that the Bernard-Soulier syndrome is heterogeneous and is probably not due to gene deletions.

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35

Drouin, J., JL McGregor, S. Parmentier, CA Izaguirre, and KJ Clemetson. "Residual amounts of glycoprotein Ib concomitant with near-absence of glycoprotein IX in platelets of Bernard-Soulier patients." Blood 72, no. 3 (1988): 1086–88. http://dx.doi.org/10.1182/blood.v72.3.1086.bloodjournal7231086.

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A study of the Bernard-Soulier syndrome in two unrelated families using different polyclonal antibodies in a sensitive immunoblot assay showed residual amounts of platelet membrane glycoprotein (GP) lb in the eight homozygotes, as well as the near-absence of GPlb beta and GPIX. The eight heterozygotes studied showed a double band pattern for GPlb and about half the normal level of GPlb beta and GPIX. Therefore, we conclude that the Bernard-Soulier syndrome is heterogeneous and is probably not due to gene deletions.

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36

Pham, Angie, and Jun Wang. "Bernard-Soulier Syndrome: An Inherited Platelet Disorder." Archives of Pathology & Laboratory Medicine 131, no. 12 (2007): 1834–36. http://dx.doi.org/10.5858/2007-131-1834-bsaipd.

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Abstract Bernard-Soulier syndrome is an inherited platelet disorder, which is transmitted in an autosomal recessive manner. This syndrome is characterized by variable thrombocytopenia and large defective platelets. Bernard-Soulier syndrome often presents early with bleeding symptoms, such as epistaxis, ecchymosis, menometrorrhagia, and gingival or gastrointestinal bleeding. Diagnosis can be confirmed by platelet aggregation studies and flow cytometry. The differential diagnosis includes the other inherited giant platelet disorders, as well as von Willebrand disease and immune thrombocytopenia

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37

Tripathi, Preeti, Karthika K. V., H. P. Pati, and Seema Tyagi. "Bernard Soulier Syndrome; A Rare Bleeding Disorder." International Journal of Medical and Dental Sciences 7, no. 1 (2018): 1642. http://dx.doi.org/10.18311/ijmds/2018/18917.

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Bleeding syndromes in the newborn are rare, but they may be life-threatening and demand immediate attention. Congenital bleeding disorders especially pose a diagnostic challenge to the clinician because of their rarity and the need to be differentiated from the other common causes of bleeding in children. We present a case of an infant presenting with bleeding symptoms early in his life (since 5 months of age) which was initially thought to be immune thrombocytopenic purpura (ITP) with low platelet count. No response to steroids and further evaluation by platelet aggregometry and flowcytometry

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38

Chakraborty, Somajita, and Debasmita Bhadra. "Bernard–Soulier syndrome (BSS) with uncontrollable menorrhagia." Asian Journal of Transfusion Science 14, no. 1 (2020): 93. http://dx.doi.org/10.4103/ajts.ajts_61_18.

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39

Kriplani, Alka, Bhawna Malhotra Singh, Ramamurti Sowbernika, and Ved Prakash Choudhry. "Successful pregnancy outcome in Bernard-Soulier syndrome." Journal of Obstetrics and Gynaecology Research 31, no. 1 (2005): 52–56. http://dx.doi.org/10.1111/j.1447-0756.2005.00240.x.

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40

Nurden, AT, V. Jallu, and P. Hourdille. "GP Ib and Bernard-Soulier platelets [letter]." Blood 73, no. 8 (1989): 2225–27. http://dx.doi.org/10.1182/blood.v73.8.2225.2225.

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41

Nurden, AT, V. Jallu, and P. Hourdille. "GP Ib and Bernard-Soulier platelets [letter]." Blood 73, no. 8 (1989): 2225–27. http://dx.doi.org/10.1182/blood.v73.8.2225.bloodjournal7382225.

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42

Ruiz-Roca, JA, RE Oñate-Sánchez, MC Cabrerizo-Merino, and FJ Rodríguez-Lozano. "Dental Extractions Management in Bernard–Soulier Syndrome." Journal of Craniofacial Surgery 26, no. 6 (2015): 2018. http://dx.doi.org/10.1097/scs.0000000000001895.

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43

Sengupta, Sivajee. "Bernard–Soulier Syndrome: An Inherited Platelet Disorder." International Journal of Human Genetics 2, no. 3 (2002): 205–7. http://dx.doi.org/10.1080/09723757.2002.11885807.

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44

Pitarch, G., A. Torrijos, T. Martínez-Menchón, J. L. Sánchez-Carazo, and J. M. Fortea. "Familial Aquagenic Urticaria and Bernard-Soulier Syndrome." Dermatology 212, no. 1 (2006): 96–97. http://dx.doi.org/10.1159/000089035.

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45

Nakagawa, Masao, Masahiko Okuno, Nobuhiko Okamoto, Hidetoshi Fujino, and Hirofumi Kato. "Bernard-Soulier syndrome associated with 22q11.2 microdeletion." American Journal of Medical Genetics 99, no. 4 (2001): 286–88. http://dx.doi.org/10.1002/1096-8628(2001)9999:9999<::aid-ajmg1176>3.0.co;2-t.

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46

Okan, V., M. Araz, C. Camci, et al. "BERNARD‐SOULIER SYNDROME IN A TURKISH FAMILY." International Journal of Clinical Practice 56, no. 7 (2002): 546–48. http://dx.doi.org/10.1111/j.1742-1241.2002.tb11316.x.

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47

CRISPOLON, ELORDE JR S., SHERYL A. YAP, and ADELINE SOULIER-PERKINS. "Revision of the endemic Philippine Poeciloterpa Stål (Hemiptera: Cercopidae) with description of four new species." Zootaxa 4608, no. 2 (2019): 291. http://dx.doi.org/10.11646/zootaxa.4608.2.6.

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The genus Poeciloterpa Stål endemic to the Philippines with 9 known species is reviewed. Four new species are described and illustrated: P. altissima Crispolon et Soulier-Perkins sp. nov., P. conica Crispolon et Soulier-Perkins sp. nov., P. gapudi Crispolon et Yap sp. nov. and P. mangkas Crispolon et Yap sp. nov. Illustrations and descriptions for the male genitalia are given for the first time for all the species except for P. nigrolimbata Stål known only by two female specimens. A key to species is provided. The type of habitats where the species are found is discussed and new host-plants li

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48

Kanaji, Taisuke, Susan Russell, and Jerry Ware. "Amelioration of the macrothrombocytopenia associated with the murine Bernard-Soulier syndrome." Blood 100, no. 6 (2002): 2102–7. http://dx.doi.org/10.1182/blood-2002-03-0997.

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Abstract An absent platelet glycoprotein (GP) Ib-IX receptor results in the Bernard-Soulier syndrome and is characterized by severe bleeding and the laboratory presentation of macrothrombocytopenia. Although the macrothrombocytopenic phenotype is directly linked to an absent GP Ib-IX complex, the disrupted molecular mechanisms that produce the macrothrombocytopenia are unknown. We have utilized a mouse model of the Bernard-Soulier syndrome to engineer platelets expressing an α-subunit of GP Ib (GP Ibα) in which most of the extracytoplasmic sequence has been replaced by an isolated domain of th

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49

Kenny, Dermot, Ólafur G. Jónsson, Patricia A. Morateck та Robert R. Montgomery. "Naturally Occurring Mutations in Glycoprotein Ibα That Result in Defective Ligand Binding and Synthesis of a Truncated Protein". Blood 92, № 1 (1998): 175–83. http://dx.doi.org/10.1182/blood.v92.1.175.413a36_175_183.

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The platelet GPIb-V-IX complex is the receptor for the initial binding of von Willebrand factor (vWF) mediating platelet adhesion. The complex is composed of four membrane-spanning glycoproteins (GP): GPIbα, GPIbβ, GPIX, and GPV. Bernard-Soulier syndrome results from a qualitative or quantitative defect in one or more components of the platelet membrane GPIb-V-IX complex. We describe the molecular basis of a novel Bernard-Soulier syndrome variant in two siblings in whom GPIbα was not detected on the platelet surface but that was present in a soluble form in plasma. DNA sequence analysis showed

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50

Perez, Amanda Vilaverde, Cilomar Martins de Oliveira Filho, Tássia Cividanes Pazinato, et al. "Bernard-Soulier Syndrome in Pregnancy: A Case Report." Open Journal of Obstetrics and Gynecology 09, no. 06 (2019): 838–44. http://dx.doi.org/10.4236/ojog.2019.96082.

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