Thematische Bibliographien / Alkaptonuria / Zeitschriftenartikel
Um die anderen Arten von Veröffentlichungen zu diesem Thema anzuzeigen, folgen Sie diesem Link: Alkaptonuria.

Zeitschriftenartikel zum Thema „Alkaptonuria“

Autor: Grafiati
Veröffentlicht am 14. März 2023

Geben Sie eine Quelle nach APA, MLA, Chicago, Harvard und anderen Zitierweisen an

Wählen Sie eine Art der Quelle aus:

Machen Sie sich mit Top-50 Zeitschriftenartikel für die Forschung zum Thema "Alkaptonuria" bekannt.

Neben jedem Werk im Literaturverzeichnis ist die Option "Zur Bibliographie hinzufügen" verfügbar. Nutzen Sie sie, wird Ihre bibliographische Angabe des gewählten Werkes nach der nötigen Zitierweise (APA, MLA, Harvard, Chicago, Vancouver usw.) automatisch gestaltet.

Sie können auch den vollen Text der wissenschaftlichen Publikation im PDF-Format herunterladen und eine Online-Annotation der Arbeit lesen, wenn die relevanten Parameter in den Metadaten verfügbar sind.

Sehen Sie die Zeitschriftenartikel für verschiedene Spezialgebieten durch und erstellen Sie Ihre Bibliographie auf korrekte Weise.

1

Tharini, GK, Vidhya Ravindran, N. Hema, D. Prabhavathy und B. Parveen. „Alkaptonuria“. Indian Journal of Dermatology 56, Nr. 2 (2011): 186. http://dx.doi.org/10.4103/0019-5154.80415.

Der volle Inhalt der Quelle
APA, Harvard, Vancouver, ISO und andere Zitierweisen
2

Bassily, Emmanuel, M. Cody O'Dell, Brad Homan und Christopher Wasyliw. „Alkaptonuria“. Orthopedics 39, Nr. 4 (09.05.2016): e810-e813. http://dx.doi.org/10.3928/01477447-20160503-03.

Der volle Inhalt der Quelle
APA, Harvard, Vancouver, ISO und andere Zitierweisen
3

Islam, Md Nazrul, SM Kamal, Sk Amir Hossain und Sirajul Islam. „Alkaptonuria“. Bangladesh Medical Journal Khulna 49, Nr. 1-2 (07.03.2017): 37–39. http://dx.doi.org/10.3329/bmjk.v49i1-2.31825.

Der volle Inhalt der Quelle
Annotation:
Alkaptonuria is a rare metabolic autosomal recessive disorder. It occurs due to lack of an enzyme that results in deposition of homogentisic acid in various tissues. A male patient of 45 years presented with back pain for 20 years and multiple joint pain for 10 years. Patient has multiple nodules in both pinnae and pigmentation in both sclerae. His urine turns black upon standing. These findings are compatible with the diagnosis of Alkaptonuria.Bang Med J (Khulna) 2016; 49 : 37-39
APA, Harvard, Vancouver, ISO und andere Zitierweisen
4

Indiran, Venkatraman, Dillibabu Ethiraj, Kanakaraj Kannan und ThirumalasettyRamachandra Prasad. „Alkaptonuria“. Indian Journal of Rheumatology 13, Nr. 3 (2018): 209. http://dx.doi.org/10.4103/injr.injr_67_18.

Der volle Inhalt der Quelle
APA, Harvard, Vancouver, ISO und andere Zitierweisen
5

Brenton, D. P., und S. Krywawych. „Alkaptonuria“. Clinics in Rheumatic Diseases 12, Nr. 3 (Dezember 1986): 755–69. http://dx.doi.org/10.1016/s0307-742x(21)00578-6.

Der volle Inhalt der Quelle
APA, Harvard, Vancouver, ISO und andere Zitierweisen
6

Mistry, Jemma B., Marwan Bukhari und Adam M. Taylor. „Alkaptonuria“. Rare Diseases 1, Nr. 1 (Januar 2013): e27475. http://dx.doi.org/10.4161/rdis.27475.

Der volle Inhalt der Quelle
APA, Harvard, Vancouver, ISO und andere Zitierweisen
7

Harper, P. S. „Alkaptonuria“. Journal of Medical Genetics 22, Nr. 2 (01.04.1985): 159. http://dx.doi.org/10.1136/jmg.22.2.159.

Der volle Inhalt der Quelle
APA, Harvard, Vancouver, ISO und andere Zitierweisen
8

Thapa, Manish, M. Bhatia und V. K. Maurya. „Alkaptonuria“. Medical Journal Armed Forces India 74, Nr. 4 (Oktober 2018): 394–96. http://dx.doi.org/10.1016/j.mjafi.2017.06.006.

Der volle Inhalt der Quelle
APA, Harvard, Vancouver, ISO und andere Zitierweisen
9

Carlesimo, M., P. Bonaccorsi, G. Tamburrano, I. Carboni, A. Parisi und S. Calvier. „Alkaptonuria“. Dermatology 199, Nr. 1 (1999): 70–71. http://dx.doi.org/10.1159/000018186.

Der volle Inhalt der Quelle
APA, Harvard, Vancouver, ISO und andere Zitierweisen
10

El-Sayed Ahmed, Magdy M., Omar Hussain, David A. Ott und Muhammad Aftab. „Severe Aortic Valve Stenosis Due to Alkaptonuric Ochronosis“. Seminars in Cardiothoracic and Vascular Anesthesia 21, Nr. 4 (14.07.2017): 364–66. http://dx.doi.org/10.1177/1089253217720284.

Der volle Inhalt der Quelle
Annotation:
Alkaptonuric ochronosis is a rare cause of aortic valve stenosis. We report the case of a 61-year-old female patient with alkaptonuria who presented to our institute with the clinical picture of severe aortic valve stenosis, which was confirmed by transthoracic echocardiography. On aortotomy, she was noted to have an impressive black discoloration of ascending aorta and the aortic root complex involving the aortic valve leaflets. She underwent an uneventful aortic valve replacement. She was discharged home 10 days postoperatively.
APA, Harvard, Vancouver, ISO und andere Zitierweisen
11

GARROD, ARCHIBALD E. „ABOUT ALKAPTONURIA“. Endocrinologist 2, Nr. 5 (September 1992): 288–90. http://dx.doi.org/10.1097/00019616-199209000-00004.

Der volle Inhalt der Quelle
APA, Harvard, Vancouver, ISO und andere Zitierweisen
12

Farzannia, Akbar, Ghaffar Shokouhi und Shahram Hadidchi. „Alkaptonuria and lumbar disc herniation“. Journal of Neurosurgery: Spine 98, Nr. 1 (Januar 2003): 87–89. http://dx.doi.org/10.3171/spi.2003.98.1.0087.

Der volle Inhalt der Quelle
Annotation:
✓ Alkaptonuria is a rare metabolic disease caused by deficiency of homogentisic acid oxidase and characterized by bluish-black discoloration of cartilages and skin (ochronosis). The authors report the cases of three patients with lumbar disc herniation who underwent discectomy and in whom the nucleus pulposus was discovered to be black. Alkaptonuria was diagnosed after discectomy. Discal herniation requiring surgery is unusual in alkaptonuria, with only a few reports. The symptoms in the three patients disappeared after surgery and no symptoms were demonstrated on follow-up examination.
APA, Harvard, Vancouver, ISO und andere Zitierweisen
13

Steven, R. A., A. J. Kinshuck, M. S. McCormick und L. R. Ranganath. „ENT manifestations of alkaptonuria: report on a case series“. Journal of Laryngology & Otology 129, Nr. 10 (Oktober 2015): 1004–8. http://dx.doi.org/10.1017/s0022215115002315.

Der volle Inhalt der Quelle
Annotation:
AbstractBackground:Alkaptonuria is an inborn error of metabolism. It is a multisystem disease with characteristic ENT manifestations. This paper reports, for the first time, the ENT findings in a cohort of alkaptonuria patients.Method:Patients attending the National Centre for Alkaptonuria (Royal Liverpool and Broadgreen University Hospitals NHS Trust) underwent a full ENT assessment.Results:Eighteen of the 20 patients (90 per cent) had an ENT sign or symptom. These included discolouration of the pinna, cerumen, nasal septum and pharynx.Conclusion:Discolouration of cerumen may occur before 30 years of age and may therefore be an important early clinical sign. Further audiological assessment of patients is needed to clarify if an association exists between alkaptonuria and hearing loss. Alkaptonuria is a condition that could present to the otolaryngologist. Successful early diagnosis and referral to a specialist centre is essential so that patients can be offered disease-modifying therapy.
APA, Harvard, Vancouver, ISO und andere Zitierweisen
14

Wiwanitkit, Viroj. „Diagnosis of alkaptonuria“. Indian Journal of Otology 18, Nr. 1 (2012): 44. http://dx.doi.org/10.4103/0971-7749.98306.

Der volle Inhalt der Quelle
APA, Harvard, Vancouver, ISO und andere Zitierweisen
15

Phatak, SV, PK Kolwadkar, TJ Hemnani, MS Phatak und JT Hemnani. „Pictorial essay: Alkaptonuria“. Indian Journal of Radiology and Imaging 16, Nr. 4 (2006): 573. http://dx.doi.org/10.4103/0971-3026.32272.

Der volle Inhalt der Quelle
APA, Harvard, Vancouver, ISO und andere Zitierweisen
16

TUNÇEZ AKYÜREK, Fatma, Özlem BİLGİÇ, Gülcan SAYLAM KURTİPEK, İlknur ALBAYRAK GEZER und Hilmi Cevdet ALTINYAZAR. „Alkaptonuria: Case Report“. Turkiye Klinikleri Journal of Dermatology 25, Nr. 3 (2015): 103–7. http://dx.doi.org/10.5336/dermato.2014-42697.

Der volle Inhalt der Quelle
APA, Harvard, Vancouver, ISO und andere Zitierweisen
17

Craide, Fernanda Helena, Juliana Salvini Barbosa Martins da Fonseca, Priscila Coelho Mariano, Natalia Monteiro Fernandez, Carlos Gustavo Carneiro de Castro und Yuri de Souza Lima Mene. „Alkaptonuria - Case report“. Anais Brasileiros de Dermatologia 89, Nr. 5 (September 2014): 799–801. http://dx.doi.org/10.1590/abd1806-4841.20143052.

Der volle Inhalt der Quelle
APA, Harvard, Vancouver, ISO und andere Zitierweisen
18

Khatu, SwapnaS, YuvrajE More, Divyank Vankawala, Deepali Chavan und NeetaR Gokhale. „Alkaptonuria: Case report“. Medical Journal of Dr. D.Y. Patil University 8, Nr. 1 (2015): 84. http://dx.doi.org/10.4103/0975-2870.148860.

Der volle Inhalt der Quelle
APA, Harvard, Vancouver, ISO und andere Zitierweisen
19

Mwambingu, Thomas L., und Geoff Hide. „Case 208: Alkaptonuria“. Radiology 272, Nr. 2 (August 2014): 608–11. http://dx.doi.org/10.1148/radiol.14121842.

Der volle Inhalt der Quelle
APA, Harvard, Vancouver, ISO und andere Zitierweisen
20

Zatkova, Andrea, Lakshminarayan Ranganath und Ludevit Kadasi. „Alkaptonuria: Current Perspectives“. Application of Clinical Genetics Volume 13 (Januar 2020): 37–47. http://dx.doi.org/10.2147/tacg.s186773.

Der volle Inhalt der Quelle
APA, Harvard, Vancouver, ISO und andere Zitierweisen
21

Anikster, Yair, William L. Nyhan und William A. Gahl. „NTBC and Alkaptonuria“. American Journal of Human Genetics 63, Nr. 3 (September 1998): 920–21. http://dx.doi.org/10.1086/302027.

Der volle Inhalt der Quelle
APA, Harvard, Vancouver, ISO und andere Zitierweisen
22

Laxon, S., L. Ranganath und O. Timmis. „Living with alkaptonuria“. BMJ 343, sep29 2 (29.09.2011): d5155. http://dx.doi.org/10.1136/bmj.d5155.

Der volle Inhalt der Quelle
APA, Harvard, Vancouver, ISO und andere Zitierweisen
23

Millucci, Lia, Daniela Braconi, Giulia Bernardini, Pietro Lupetti, Josef Rovensky, Lakshminaryan Ranganath und Annalisa Santucci. „Amyloidosis in alkaptonuria“. Journal of Inherited Metabolic Disease 38, Nr. 5 (14.04.2015): 797–805. http://dx.doi.org/10.1007/s10545-015-9842-8.

Der volle Inhalt der Quelle
APA, Harvard, Vancouver, ISO und andere Zitierweisen
24

Millucci, Lia, Giulia Bernardini, Barbara Marzocchi, Daniela Braconi, Michela Geminiani, Silvia Gambassi, Marcella Laschi et al. „Angiogenesis in alkaptonuria“. Journal of Inherited Metabolic Disease 39, Nr. 6 (26.09.2016): 801–6. http://dx.doi.org/10.1007/s10545-016-9976-3.

Der volle Inhalt der Quelle
APA, Harvard, Vancouver, ISO und andere Zitierweisen
25

Denisova, E. V., und A. V. Kuzin. „Ophthalmological Manifestations of Alkaptonuria“. Ophthalmology in Russia 19, Nr. 1 (08.04.2022): 118–22. http://dx.doi.org/10.18008/1816-5095-2022-1-118-122.

Der volle Inhalt der Quelle
Annotation:
Alkaptonuria is rare autosomal recessive multisystem disease, caused by mutations in the homogentisine oxidase gene, which leads to the deposition of metabolites of homogentisic acid in organs and tissues (ochronosis).The purpose: to study spectrum of ophthalmic manifestations of alkaptonuria in Russian cohort of patients of different ages.Material and methods. Ophthalmological examination of 9 patients: 5 adults aged from 39 to 64 years and 4 children aged from 3 to 6 years with confirmed diagnosis of “alkaptonuria” was performed.Results. In all adult patients bilateral brown-black scleral pigmentation and yellow-brown deposits in the conjunctiva in the region of the palpebral fissure were detected paralymbally, the severity of which correlated with age, tortuosity and vasodilation of the conjunctiva in areas of deposits. In 1 out of 4 children minimal deposits of yellow pigment were found in the conjunctiva of the limb. In patients older than 60 years typical small brownish deposits were observed in the cornea near the limb in the region of the palpebral fissure.Conclusion. Eye changes are one of the most common clinical manifestations of alkaptonuria. Typical manifestations are the sclera’s pigmentation, conjunctiva and cornea in the limb. Ophthalmological examination is non-invasive informative method that can help in early diagnosis, differential diagnostics, assessment of the dynamics of the disease and the effectiveness of the therapy.
APA, Harvard, Vancouver, ISO und andere Zitierweisen
26

Menon, I. Aravind, Suruj D. Persad, Herbert F. Haberman, Prasanta K. Basu, Joseph F. Norfray, Christopher C. Felix und B. Kalyanaraman. „Characterization of the pigment from homogentisic acid and urine and tissue from an alkaptonuria patient“. Biochemistry and Cell Biology 69, Nr. 4 (01.04.1991): 269–73. http://dx.doi.org/10.1139/o91-041.

Der volle Inhalt der Quelle
Annotation:
When urine samples from alkaptonuria patients are allowed to stand, they turn black, presumably owing to the oxidation of homogentisic acid to a melanin-like substance. We report the characterization of the pigments formed by polymerization of (a) the components in the urine from a patient with alkaptonuria and (b) homogentisic acid. The absorption spectra and electron spin resonance signals of these pigments are similar to those of eumelanins. Irradiation of the pigments with nitroblue tetrazolium caused reduction of the tetrazolium; this was partially inhibited by superoxide dismutase. Irradiation of Ehrlich ascites carcinoma cells with the pigments from homogentisic acid or urine caused cell lysis. Since this lysis was inhibited by catalase, we have concluded that it was mediated by H2O2. A similar pigment was also extracted from the tissue from an alkaptonuria patient. It is suggested that the degeneration of tissue in vivo may be due to the deposition of melanin-like pigments in the tissues, probably in combination with metal ions.Key words: alkaptonuria, homogentisic acid, pigmentation, melanin, photosensitization.
APA, Harvard, Vancouver, ISO und andere Zitierweisen
27

Shah, Anand, Andrew Son und Payam Salehi. „Alkaptonuric ochronosis of the carotid artery“. SAGE Open Medical Case Reports 8 (Januar 2020): 2050313X2091541. http://dx.doi.org/10.1177/2050313x20915411.

Der volle Inhalt der Quelle
Annotation:
Alkaptonuria is a rare autosomal-recessive metabolic disorder of tyrosine degradation which results in elevated levels of circulating homogentisic acid. Ochronosis occurs when homogentisic acid polymerizes and deposits in connective tissue. Ochronotic lesions in the carotid arteries have not been described. In this report, we describe a 65-year-old man with alkaptonuria, with hypertension and hyperlipidemia, who underwent an uneventful carotid endarterectomy for an asymptomatic high-grade internal carotid artery stenosis. Histology revealed homogentisic acid deposits as black-brownish areas in the intima. He was noted to have an impressive heavily brown-black pigmented discoloration of the carotid plaque. Cardiovascular involvement is a rare consequence of alkaptonuria and is manifested by pigment deposition at the areas influenced by shear stress and turbulence.
APA, Harvard, Vancouver, ISO und andere Zitierweisen
28

Sagit, M., M. Uludag und I. San. „An unusual dark pigmentation on the tympanic membrane“. Journal of Laryngology & Otology 125, Nr. 10 (05.08.2011): 1059–61. http://dx.doi.org/10.1017/s0022215111001903.

Der volle Inhalt der Quelle
Annotation:
AbstractObjective:To report an extremely rare case of dark pigmentation on the tympanic membrane due to alkaptonuria, and to discuss the probable association between this condition and hearing loss.Case report:A 58-year-old man with alkaptonuria was admitted with tinnitus and hearing loss in both ears. Physical examination showed bluish-black pigmentation on the helixes of both ears and both sclerae. Otoscopic examination revealed dark discolouration of both tympanic membranes. Audiological evaluation revealed mixed high frequency hearing loss in both ears. Tympanometric examination revealed type A tympanograms bilaterally, and absence of acoustic reflexes both ipsilaterally and contralaterally. Computed tomography of the temporal bones revealed no abnormality.Conclusion:Clinicians should consider alkaptonuria in the differential diagnosis of patients with abnormal tympanic membrane pigmentation and hearing loss.
APA, Harvard, Vancouver, ISO und andere Zitierweisen
29

Khalil, Raida, Dema Ali, Nesrin Mwafi, Arwa Alsaraireh, Loiy Obeidat, Eman Albsoul und Ibrahim Al Sbou’. „Variant Analysis of Alkaptonuria Families with Significant Founder Effect in Jordan“. BioMed Research International 2021 (11.03.2021): 1–8. http://dx.doi.org/10.1155/2021/1515641.

Der volle Inhalt der Quelle
Annotation:
Background. Metabolic disorder alkaptonuria is an autosomal recessive disorder caused by mutations in the HGD gene, and a deficiency HGD enzyme activity results in an accumulation of homogentisic acid (HGA), ochronosis, and destruction of connective tissue. Methods. We clinically evaluated 18 alkaptonuria patients (age range, 3 to 60 years) from four unrelated families. Furthermore, 11 out of 18 alkaptonuria patients and 7 unaffected members were enrolled for molecular investigations by utilizing Sanger sequencing to identify variants of the 14 exons of HGD gene. Results. We found that the seven patients from the 4 unrelated families carried a recurrent pathogenic missense variant (c.365C>T, p. Ala122Val) in exon 6 of HGD gene. The variant was fully segregated with the disease in affected family members while the other unaffected family members were heterozygous carriers for this variant. Additionally, the clinical features were fully predicted with alkaptonuria disorder. Conclusion. In this study, we confirmed that the most common variants in Jordanian AKU patients was c.365C>T, p. Ala122Val in exon 6 of HGD gene. Additionally, we correlated the clinical and genetic features of AKU patients at various ages (3-60 years).
APA, Harvard, Vancouver, ISO und andere Zitierweisen
30

Damarla, Nirupama, Prathima Linga, Mallika Goyal, SanjayReddy Tadisina, GSatyanarayana Reddy und Hymavathi Bommisetti. „Alkaptonuria: A case report“. Indian Journal of Ophthalmology 65, Nr. 6 (2017): 518. http://dx.doi.org/10.4103/ijo.ijo_337_16.

Der volle Inhalt der Quelle
APA, Harvard, Vancouver, ISO und andere Zitierweisen
31

Yasri, Sora, und Viroj Wiwanitkit. „ß-thalassemia and alkaptonuria“. Indian Journal of Human Genetics 20, Nr. 1 (2014): 97. http://dx.doi.org/10.4103/0971-6866.132772.

Der volle Inhalt der Quelle
APA, Harvard, Vancouver, ISO und andere Zitierweisen
32

Verma, ShyamB. „Early detection of alkaptonuria“. Indian Journal of Dermatology, Venereology and Leprology 71, Nr. 3 (2005): 189. http://dx.doi.org/10.4103/0378-6323.16236.

Der volle Inhalt der Quelle
APA, Harvard, Vancouver, ISO und andere Zitierweisen
33

Laurent, James P., und Sean D. Galvin. „Black Aorta from Alkaptonuria“. AORTA 09, Nr. 04 (August 2021): 165–66. http://dx.doi.org/10.1055/s-0041-1729916.

Der volle Inhalt der Quelle
Annotation:
AbstractA-76-year old male with a past history of alkaptonuria with ochronosis (homogentisic acid deposition in tissues) had symptomatic aortic stenosis. Surgical replacement of the valve was undertaken, and he was noted to have a severely pigmented and porcelain aorta.
APA, Harvard, Vancouver, ISO und andere Zitierweisen
34

Khan, Aysha Habib, Bushra Afroze, Hafsa Majid, Yusra Zaidi, Azeema Jamil und Lena Jafri. „Musculoskeletal manifestations in Alkaptonuria“. Medicine 100, Nr. 51 (23.12.2021): e28241. http://dx.doi.org/10.1097/md.0000000000028241.

Der volle Inhalt der Quelle
APA, Harvard, Vancouver, ISO und andere Zitierweisen
35

Trotsenko, V. V., V. I. Nuzhdin, T. P. Popova, S. V. Kagramanov, O. A. Kudinov und A. S. Bavashev. „Alkaptonuria and ochronotic arthropathy“. N.N. Priorov Journal of Traumatology and Orthopedics 9, Nr. 1 (02.02.2022): 63–66. http://dx.doi.org/10.17816/vto97136.

Der volle Inhalt der Quelle
Annotation:
Four cases of operative treatment for ochronosis arthropathy in patients with alcaptonuria are presented. In 3 patients hip joint and in 1 patient knee joint were affected. Prior to surgery all patients were treated conservatively. Two patients successfully underwent total hip replacement. Intertrochanteric femur osteotomy was performed in 1 case. In the fourth patient arthroplasty of knee joint with allograft from rib cartilage failed due to suppurative arthritis resulted in joint resection and arthrodesis.
APA, Harvard, Vancouver, ISO und andere Zitierweisen
36

Gilmullin, I. F., und A. Sh Latypov. „A case of alkaptonuria“. Kazan medical journal 68, Nr. 1 (15.02.1987): 63–64. http://dx.doi.org/10.17816/kazmj95911.

Der volle Inhalt der Quelle
Annotation:
Insignificant population frequency of alkaptonuria - 3-5 per 1,000,000 (H.P. Bochkov et al., 1984), autosomal recessive character of inheritance, which often does not give family accumulation, late development of clinical symptoms (after 40 years) lead to that practical doctors, rarely meeting with the specified pathology and having no indication of family or congenital character of the disease, find it difficult to make a diagnosis.
APA, Harvard, Vancouver, ISO und andere Zitierweisen
37

VLAY, STEPHEN C. „Alkaptonuria and Aortic Stenosis“. Annals of Internal Medicine 104, Nr. 3 (01.03.1986): 446. http://dx.doi.org/10.7326/0003-4819-104-3-446_1.

Der volle Inhalt der Quelle
APA, Harvard, Vancouver, ISO und andere Zitierweisen
38

Akeda, Koji, Yuichi Kasai, Eiji Kawakita, Yoshihiro Matsumura, Toshibumi Kono, Tetsuya Murata und Atsumasa Uchida. „Thoracic Myelopathy With Alkaptonuria“. Spine 33, Nr. 2 (Januar 2008): E62—E65. http://dx.doi.org/10.1097/brs.0b013e31816046ea.

Der volle Inhalt der Quelle
APA, Harvard, Vancouver, ISO und andere Zitierweisen
39

Odabas, Ali Riza, Ali Karakuzu, Yilmaz Selcuk, Teoman Erdem und Ramazan Cetinkaya. „Alkaptonuria: A Case Report“. Journal of Dermatology 28, Nr. 3 (März 2001): 158–60. http://dx.doi.org/10.1111/j.1346-8138.2001.tb00111.x.

Der volle Inhalt der Quelle
APA, Harvard, Vancouver, ISO und andere Zitierweisen
40

Gehrig, A., S. R. Schmidt, C. R. Müller, S. Srsen, K. Srsnova und W. Kress. „Molecular defects in alkaptonuria“. Cytogenetic and Genome Research 76, Nr. 1-2 (1997): 14–16. http://dx.doi.org/10.1159/000134501.

Der volle Inhalt der Quelle
APA, Harvard, Vancouver, ISO und andere Zitierweisen
41

Thimmapuram, Rashmi, W. Patricia Bandettini, Sujata M. Shanbhag, Jeannie H. Yu, Kevin J. O'Brien, William A. Gahl, Wendy J. Introne und Marcus Y. Chen. „Aortic distensibility in alkaptonuria“. Molecular Genetics and Metabolism 130, Nr. 4 (August 2020): 289–96. http://dx.doi.org/10.1016/j.ymgme.2020.05.006.

Der volle Inhalt der Quelle
APA, Harvard, Vancouver, ISO und andere Zitierweisen
42

Phornphutkul, Chanika, Wendy J. Introne, Monique B. Perry, Isa Bernardini, Mark D. Murphey, Diana L. Fitzpatrick, Paul D. Anderson et al. „Natural History of Alkaptonuria“. New England Journal of Medicine 347, Nr. 26 (26.12.2002): 2111–21. http://dx.doi.org/10.1056/nejmoa021736.

Der volle Inhalt der Quelle
APA, Harvard, Vancouver, ISO und andere Zitierweisen
43

M B, Adarsh, Saket Jha, Preksha Dwivedi und Sanjay Jain. „A Mistaken Identity—Alkaptonuria“. JCR: Journal of Clinical Rheumatology 26, Nr. 5 (23.04.2019): e147-e148. http://dx.doi.org/10.1097/rhu.0000000000001044.

Der volle Inhalt der Quelle
APA, Harvard, Vancouver, ISO und andere Zitierweisen
44

Kamoun, P., M. Coude, M. Forest, X. Montagutelli und J. L. Guenet. „Ascorbic acid and alkaptonuria“. European Journal of Pediatrics 151, Nr. 2 (Februar 1992): 149. http://dx.doi.org/10.1007/bf01958966.

Der volle Inhalt der Quelle
APA, Harvard, Vancouver, ISO und andere Zitierweisen
45

Lok, Zoe S. Y., Jacob Goldstein und Julian A. Smith. „Alkaptonuria-Associated Aortic Stenosis“. Journal of Cardiac Surgery 28, Nr. 4 (Juli 2013): 417–20. http://dx.doi.org/10.1111/jocs.12129.

Der volle Inhalt der Quelle
APA, Harvard, Vancouver, ISO und andere Zitierweisen
46

Pettit, Stephen J., Michael Fisher, James A. Gallagher und Lakshminarayan R. Ranganath. „Cardiovascular manifestations of Alkaptonuria“. Journal of Inherited Metabolic Disease 34, Nr. 6 (20.04.2011): 1177–81. http://dx.doi.org/10.1007/s10545-011-9339-z.

Der volle Inhalt der Quelle
APA, Harvard, Vancouver, ISO und andere Zitierweisen
47

Cox, Timothy M. „Alkaptonuria: treasure your exceptions“. Journal of Inherited Metabolic Disease 34, Nr. 6 (22.09.2011): 1113–14. http://dx.doi.org/10.1007/s10545-011-9385-6.

Der volle Inhalt der Quelle
APA, Harvard, Vancouver, ISO und andere Zitierweisen
48

Mori, Yotaro, Noriyuki Takashima, Shunta Miwa, Yuji Matsubayashi, Naoshi Minamidate, Masahide Enomoto, Kenichi Kamiya und Tomoaki Suzuki. „Aortic Stenosis with Alkaptonuria“. Japanese Journal of Cardiovascular Surgery 51, Nr. 6 (15.11.2022): 350–53. http://dx.doi.org/10.4326/jjcvs.51.350.

Der volle Inhalt der Quelle
APA, Harvard, Vancouver, ISO und andere Zitierweisen
49

Liu, Wendy, und Richard A. Prayson. „Dura Mater Involvement in Ochronosis (Alkaptonuria)“. Archives of Pathology & Laboratory Medicine 125, Nr. 7 (01.07.2001): 961–63. http://dx.doi.org/10.5858/2001-125-0961-dmiioa.

Der volle Inhalt der Quelle
Annotation:
Abstract Clinical manifestations of alkaptonuria have been well described and are most commonly characterized by ochronosis or pigmentation of connective tissue. Sites most commonly involved in ochronosis include joints, heart, skin, and kidney. We describe a 66-year-old woman with a history of alkaptonuria who had widespread ochronosis. The dura mater showed extensive pigment deposition, which was evident both grossly and microscopically at autopsy. To our knowledge, description of dura mater involvement by ochronosis has not been previously reported in the literature.
APA, Harvard, Vancouver, ISO und andere Zitierweisen
50

Rathore, Farooq A., Saeed B. Ayaz und Sahibzada N. Mansoor. „Ochronotic Arthropathy: Two Case Reports from a Developing Country“. Clinical Medicine Insights: Arthritis and Musculoskeletal Disorders 9 (Januar 2016): CMAMD.S31560. http://dx.doi.org/10.4137/cmamd.s31560.

Der volle Inhalt der Quelle
Annotation:
Alkaptonuria is a rare inborn error of metabolism, which is classified as an orphan disease. It is due to the lack of an enzyme homogentisate 1,2-dioxygenase, which results in an accumulation of homogentisic acid in different areas of the body, including sclera, skin, cardiac valves, articular cartilage of the large joints and intervertebral disks. We present two cases of alkaptonuria resulting in ochronotic arthropathy with advanced secondary generalized osteoarthritis, intervertebral disk calcifications, skin and scleral pigmentation. In these case reports, both patients had symptoms for >10 years before being diagnosed. Conservative management in the form of high-dose ascorbic acid, exercises, and gait aids was offered to both of them, which resulted in some symptomatic improvement in the first case, while the second case was lost to follow-up. Alkaptonuria is a rare disease, and although it does not clearly impact mortality, early diagnosis may improve the quality of life.
APA, Harvard, Vancouver, ISO und andere Zitierweisen
Wir bieten Rabatte auf alle Premium-Pläne für Autoren, deren Werke in thematische Literatursammlungen aufgenommen wurden. Kontaktieren Sie uns, um einen einzigartigen Promo-Code zu erhalten!

Zur Bibliographie