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215 results

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Page 1
Genetic identity of Marinesco-Sjögren/myoglobinuria and CCFDN syndromes.
Merlini L, Gooding R, Lochmüller H, Müller-Felber W, Walter MC, Angelicheva D, Talim B, Hallmayer J, Kalaydjieva L. Merlini L, et al. Among authors: hallmayer j. Neurology. 2002 Jan 22;58(2):231-6. doi: 10.1212/wnl.58.2.231. Neurology. 2002. PMID: 11805249
Gene mapping in Gypsies identifies a novel demyelinating neuropathy on chromosome 8q24.
Kalaydjieva L, Hallmayer J, Chandler D, Savov A, Nikolova A, Angelicheva D, King RH, Ishpekova B, Honeyman K, Calafell F, Shmarov A, Petrova J, Turnev I, Hristova A, Moskov M, Stancheva S, Petkova I, Bittles AH, Georgieva V, Middleton L, Thomas PK. Kalaydjieva L, et al. Among authors: hallmayer j. Nat Genet. 1996 Oct;14(2):214-7. doi: 10.1038/ng1096-214. Nat Genet. 1996. PMID: 8841199
A founder mutation in the GK1 gene is responsible for galactokinase deficiency in Roma (Gypsies).
Kalaydjieva L, Perez-Lezaun A, Angelicheva D, Onengut S, Dye D, Bosshard NU, Jordanova A, Savov A, Yanakiev P, Kremensky I, Radeva B, Hallmayer J, Markov A, Nedkova V, Tournev I, Aneva L, Gitzelmann R. Kalaydjieva L, et al. Among authors: hallmayer j. Am J Hum Genet. 1999 Nov;65(5):1299-307. doi: 10.1086/302611. Am J Hum Genet. 1999. PMID: 10521295 Free PMC article.
Bipolar disorder in the Bulgarian Gypsies: genetic heterogeneity in a young founder population.
Kaneva R, Milanova V, Angelicheva D, MacGregor S, Kostov C, Vladimirova R, Aleksiev S, Angelova M, Stoyanova V, Loh A, Hallmayer J, Kalaydjieva L, Jablensky A. Kaneva R, et al. Among authors: hallmayer j. Am J Med Genet B Neuropsychiatr Genet. 2009 Mar 5;150B(2):191-201. doi: 10.1002/ajmg.b.30775. Am J Med Genet B Neuropsychiatr Genet. 2009. PMID: 18444255
Genetic heterogeneity of polycystic kidney disease in Bulgaria.
Bogdanova N, Dworniczak B, Dragova D, Todorov V, Dimitrakov D, Kalinov K, Hallmayer J, Horst J, Kalaydjieva L. Bogdanova N, et al. Among authors: hallmayer j. Hum Genet. 1995 Jun;95(6):645-50. doi: 10.1007/BF00209481. Hum Genet. 1995. PMID: 7789949
Angiotensin-converting enzyme activity and the ACE Alu polymorphism in autosomal dominant polycystic kidney disease.
Schiavello T, Burke V, Bogdanova N, Jasik P, Melsom S, Boudville N, Robertson K, Angelicheva D, Dworniczak B, Lemmens M, Horst J, Todorov V, Dimitrakov D, Sulowicz W, Krasniak A, Stompor T, Beilin L, Hallmayer J, Kalaydjieva L, Thomas M. Schiavello T, et al. Among authors: hallmayer j. Nephrol Dial Transplant. 2001 Dec;16(12):2323-7. doi: 10.1093/ndt/16.12.2323. Nephrol Dial Transplant. 2001. PMID: 11733623
A linkage study of affective disorders in two Bulgarian Gypsy families: results for candidate regions on chromosomes 18 and 21.
Kaneva R, Milanova V, Onchev G, Stoyanova V, Chakarova CH, Nikolova A, Hallmayer J, Belemezova M, Milenska T, Kirov G, Kremensky I, Kalaydjieva L, Jablensky A. Kaneva R, et al. Among authors: hallmayer j. Psychiatr Genet. 1998 Winter;8(4):245-9. doi: 10.1097/00041444-199808040-00008. Psychiatr Genet. 1998. PMID: 9861644 No abstract available.
215 results