85 related articles for article (PubMed ID: 9888997)
1. Fine-structure mapping of the hereditary inclusion body myopathy locus.
Eisenberg I; Thiel C; Levi T; Tiram E; Argov Z; Sadeh M; Jackson CL; Thierfelder L; Mitrani-Rosenbaum S
Genomics; 1999 Jan; 55(1):43-8. PubMed ID: 9888997
[TBL] [Abstract][Full Text] [Related]
2. Various types of hereditary inclusion body myopathies map to chromosome 9p1-q1.
Argov Z; Tiram E; Eisenberg I; Sadeh M; Seidman CE; Seidman JG; Karpati G; Mitrani-Rosenbaum S
Ann Neurol; 1997 Apr; 41(4):548-51. PubMed ID: 9124813
[TBL] [Abstract][Full Text] [Related]
3. The UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase gene is mutated in recessive hereditary inclusion body myopathy.
Eisenberg I; Avidan N; Potikha T; Hochner H; Chen M; Olender T; Barash M; Shemesh M; Sadeh M; Grabov-Nardini G; Shmilevich I; Friedmann A; Karpati G; Bradley WG; Baumbach L; Lancet D; Asher EB; Beckmann JS; Argov Z; Mitrani-Rosenbaum S
Nat Genet; 2001 Sep; 29(1):83-7. PubMed ID: 11528398
[TBL] [Abstract][Full Text] [Related]
4. Physical and transcriptional map of the hereditary inclusion body myopathy locus on chromosome 9p12-p13.
Eisenberg I; Hochner H; Shemesh M; Levi T; Potikha T; Sadeh M; Argov Z; Jackson CL; Mitrani-Rosenbaum S
Eur J Hum Genet; 2001 Jul; 9(7):501-9. PubMed ID: 11464241
[TBL] [Abstract][Full Text] [Related]
5. Gene locus for autosomal recessive distal myopathy with rimmed vacuoles maps to chromosome 9.
Ikeuchi T; Asaka T; Saito M; Tanaka H; Higuchi S; Tanaka K; Saida K; Uyama E; Mizusawa H; Fukuhara N; Nonaka I; Takamori M; Tsuji S
Ann Neurol; 1997 Apr; 41(4):432-7. PubMed ID: 9124799
[TBL] [Abstract][Full Text] [Related]
6. Hereditary inclusion body myopathy maps to chromosome 9p1-q1.
Mitrani-Rosenbaum S; Argov Z; Blumenfeld A; Seidman CE; Seidman JG
Hum Mol Genet; 1996 Jan; 5(1):159-163. PubMed ID: 8789455
[TBL] [Abstract][Full Text] [Related]
7. Linkage disequilibrium in inbred North African families allows fine genetic and physical mapping of triple A syndrome.
Hadj-Rabia S; Salomon R; Pelet A; Penet C; Rotschild A; de Laët MH; Chaouachi B; Hannachi R; Bakiri F; Brauner R; Chaussain JL; Munnich A; Lyonnet S
Eur J Hum Genet; 2000 Aug; 8(8):613-20. PubMed ID: 10951524
[TBL] [Abstract][Full Text] [Related]
8. [Distal myopathy with rimmed vacuoles(DMRV)].
Ikeuchi T; Tsuji S
Nihon Rinsho; 1997 Dec; 55(12):3195-9. PubMed ID: 9436435
[TBL] [Abstract][Full Text] [Related]
9. Hereditary inclusion body myopathy: the Middle Eastern genetic cluster.
Argov Z; Eisenberg I; Grabov-Nardini G; Sadeh M; Wirguin I; Soffer D; Mitrani-Rosenbaum S
Neurology; 2003 May; 60(9):1519-23. PubMed ID: 12743242
[TBL] [Abstract][Full Text] [Related]
10. Allelic heterogeneity of GNE gene mutation in two Tunisian families with autosomal recessive inclusion body myopathy.
Amouri R; Driss A; Murayama K; Kefi M; Nishino I; Hentati F
Neuromuscul Disord; 2005 May; 15(5):361-3. PubMed ID: 15833430
[TBL] [Abstract][Full Text] [Related]
11. Mitochondrial processes are impaired in hereditary inclusion body myopathy.
Eisenberg I; Novershtern N; Itzhaki Z; Becker-Cohen M; Sadeh M; Willems PH; Friedman N; Koopman WJ; Mitrani-Rosenbaum S
Hum Mol Genet; 2008 Dec; 17(23):3663-74. PubMed ID: 18723858
[TBL] [Abstract][Full Text] [Related]
12. Mutations spectrum of GNE in hereditary inclusion body myopathy sparing the quadriceps.
Eisenberg I; Grabov-Nardini G; Hochner H; Korner M; Sadeh M; Bertorini T; Bushby K; Castellan C; Felice K; Mendell J; Merlini L; Shilling C; Wirguin I; Argov Z; Mitrani-Rosenbaum S
Hum Mutat; 2003 Jan; 21(1):99. PubMed ID: 12497639
[TBL] [Abstract][Full Text] [Related]
13. Novel GNE mutations in Italian families with autosomal recessive hereditary inclusion-body myopathy.
Broccolini A; Ricci E; Cassandrini D; Gliubizzi C; Bruno C; Tonoli E; Silvestri G; Pescatori M; Rodolico C; Sinicropi S; Servidei S; Zara F; Minetti C; Tonali PA; Mirabella M
Hum Mutat; 2004 Jun; 23(6):632. PubMed ID: 15146476
[TBL] [Abstract][Full Text] [Related]
14. Refined mapping of the CSNU3 gene to a 1.8-Mb region on chromosome 19q13.1 using historical recombinants in Libyan Jewish cystinuria patients.
Pras E; Kreiss Y; Frishberg Y; Prosen L; Aksentijevich I; Kastner DL
Genomics; 1999 Sep; 60(2):248-50. PubMed ID: 10486219
[TBL] [Abstract][Full Text] [Related]
15. Clinical delineation and localization to chromosome 9p13.3-p12 of a unique dominant disorder in four families: hereditary inclusion body myopathy, Paget disease of bone, and frontotemporal dementia.
Kovach MJ; Waggoner B; Leal SM; Gelber D; Khardori R; Levenstien MA; Shanks CA; Gregg G; Al-Lozi MT; Miller T; Rakowicz W; Lopate G; Florence J; Glosser G; Simmons Z; Morris JC; Whyte MP; Pestronk A; Kimonis VE
Mol Genet Metab; 2001 Dec; 74(4):458-75. PubMed ID: 11749051
[TBL] [Abstract][Full Text] [Related]
16. Dating the origin of the V170M mutation causing non-type I cystinuria in Libyan Jews by linkage disequilibrium and physical mapping of the SLC7A9 gene.
Colombo R
Genomics; 2000 Oct; 69(1):131-4. PubMed ID: 11013083
[TBL] [Abstract][Full Text] [Related]
17. Single nucleotide polymorphisms in the dystroglycan gene do not correlate with disease severity in hereditary inclusion body myopathy.
Gottlieb E; Ciccone C; Darvish D; Naiem-Cohen S; Dalakas MC; Savelkoul PJ; Krasnewich DM; Gahl WA; Huizing M
Mol Genet Metab; 2005; 86(1-2):244-9. PubMed ID: 16112887
[TBL] [Abstract][Full Text] [Related]
18. Homozygosity and linkage disequilibrium mapping of autosomal recessive distal myopathy (Nonaka distal myopathy).
Asaka T; Ikeuchi K; Okino S; Takizawa Y; Satake R; Nitta E; Komai K; Endo K; Higuchi S; Oyake T; Yoshimura T; Suenaga A; Uyama E; Saito T; Konagaya M; Sunohara N; Namba R; Takada H; Honke K; Nishina M; Tanaka H; Shinagawa M; Tanaka K; Matsushima A; Tsuji S; Takamori M
J Hum Genet; 2001; 46(11):649-55. PubMed ID: 11721884
[TBL] [Abstract][Full Text] [Related]
19. An Italian family with autosomal recessive quadriceps-sparing inclusion-body myopathy (ARQS-IBM) linked to chromosome 9p1.
Mirabella M; Christodoulou K; Di Giovanni S; Ricci E; Tonali P; Servidei S
Neurol Sci; 2000 Apr; 21(2):99-102. PubMed ID: 10938188
[TBL] [Abstract][Full Text] [Related]
20. Inclusion body myopathy and Paget disease is linked to a novel mutation in the VCP gene.
Haubenberger D; Bittner RE; Rauch-Shorny S; Zimprich F; Mannhalter C; Wagner L; Mineva I; Vass K; Auff E; Zimprich A
Neurology; 2005 Oct; 65(8):1304-5. PubMed ID: 16247064
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
