These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
123 related articles for article (PubMed ID: 8708653)
21. A new type of hereditary motor and sensory neuropathy linked to chromosome 3. Takashima H; Nakagawa M; Nakahara K; Suehara M; Matsuzaki T; Higuchi I; Higa H; Arimura K; Iwamasa T; Izumo S; Osame M Ann Neurol; 1997 Jun; 41(6):771-80. PubMed ID: 9189038 [TBL] [Abstract][Full Text] [Related]
22. Muscle pathology of hereditary motor and sensory neuropathy with proximal dominant involvement with TFG mutation. Yamashita S; Kimura E; Zhang Z; Tawara N; Hara K; Yoshimura A; Takashima H; Ando Y Muscle Nerve; 2019 Dec; 60(6):739-744. PubMed ID: 31449671 [TBL] [Abstract][Full Text] [Related]
23. [Two cases of hereditary motor and sensory neuropathy with proximal dominant involvement (HMSN-P)]. Mori C; Saito T; Saito T; Fujimura H; Sakoda S Rinsho Shinkeigaku; 2015; 55(6):401-5. PubMed ID: 26103812 [TBL] [Abstract][Full Text] [Related]
24. Familial optic atrophy with sex-influenced severity. A new variety of autosomal-dominant optic atrophy? Gorgone G; Li Volti S; Cavallaro N; Conti L; Profeta GM; Mollica F Ophthalmologica; 1986; 192(1):28-33. PubMed ID: 3703478 [TBL] [Abstract][Full Text] [Related]
25. [Survey of patients with advanced-stage Okinawa-type neurogenic muscular atrophy (hereditary motor and sensory neuropathy with proximal dominant involvement: HMSN-P)]. Taniguchi M; Yorishima Y; Shoji H; Ide M; Kumura Y; Kunisaki K Rinsho Shinkeigaku; 2022 Feb; 62(2):152-156. PubMed ID: 35095044 [TBL] [Abstract][Full Text] [Related]
26. Autosomal recessive type II hereditary motor and sensory neuropathy with acrodystrophy. Thomas PK; Claus D; King RH J Neurol; 1999 Feb; 246(2):107-12. PubMed ID: 10195405 [TBL] [Abstract][Full Text] [Related]
27. Varying occurrence of vocal cord paralysis in a family with autosomal dominant hereditary motor and sensory neuropathy. Donaghy M; Kennett R J Neurol; 1999 Jul; 246(7):552-5. PubMed ID: 10463355 [TBL] [Abstract][Full Text] [Related]
28. [Hereditary motor and sensory neuropathy with proximal dominant involvement (HMSN-P) is caused by a mutation in TFG]. Ishiura H; Tsuji S Rinsho Shinkeigaku; 2013; 23(11):1203-5. PubMed ID: 24291930 [TBL] [Abstract][Full Text] [Related]
29. [A family with autosomal dominant temporal lobe epilepsy accompanied by motor and sensory neuropathy]. Matsuoka T; Furuya H; Ikezoe K; Murai H; Ohyagi Y; Yoshiura T; Sasaki M; Tobimatsu S; Kira J Rinsho Shinkeigaku; 2004 Jan; 44(1):43-9. PubMed ID: 15199738 [TBL] [Abstract][Full Text] [Related]
31. Refinement of a locus for autosomal dominant hereditary motor and sensory neuropathy with proximal dominancy (HMSN-P) and genetic heterogeneity. Maeda K; Kaji R; Yasuno K; Jambaldorj J; Nodera H; Takashima H; Nakagawa M; Makino S; Tamiya G J Hum Genet; 2007; 52(11):907-914. PubMed ID: 17906970 [TBL] [Abstract][Full Text] [Related]
32. [Duffy blood groups and HLA antigens in hereditary motor-sensory neuropathy]. Nevsímalová S; Prazák J; Herzog P; Seemanová E Cesk Neurol Neurochir; 1989 Oct; 52(6):409-16. PubMed ID: 2635080 [TBL] [Abstract][Full Text] [Related]
33. Hereditary motor and sensory neuropathy with congenital glaucoma. Report on a family. Arruda WO; Comerlato EA; Scola RH; Silvado CE; Werneck LC Arq Neuropsiquiatr; 1999 Jun; 57(2A):190-4. PubMed ID: 10412516 [TBL] [Abstract][Full Text] [Related]
34. Novel mutation in the myelin protein zero gene in a family with intermediate hereditary motor and sensory neuropathy. Mastaglia FL; Nowak KJ; Stell R; Phillips BA; Edmondston JE; Dorosz SM; Wilton SD; Hallmayer J; Kakulas BA; Laing NG J Neurol Neurosurg Psychiatry; 1999 Aug; 67(2):174-9. PubMed ID: 10406984 [TBL] [Abstract][Full Text] [Related]
35. SPOAN syndrome: a novel mutation and new ocular findings; a case report. Bazvand F; Keramatipour M; Riazi-Esfahani H; Mahmoudi A BMC Neurol; 2021 Jan; 21(1):24. PubMed ID: 33451298 [TBL] [Abstract][Full Text] [Related]
36. Hereditary optic atrophy with probable association with a specific HLA haplotype. Stendahl-Brodin L; Möller E; Link H J Neurol Sci; 1978 Aug; 38(1):11-21. PubMed ID: 151734 [TBL] [Abstract][Full Text] [Related]
37. Recessive optic atrophy, sensorimotor neuropathy and cataract associated with novel compound heterozygous mutations in OPA1. Lee J; Jung SC; Hong YB; Yoo JH; Koo H; Lee JH; Hong HD; Kim SB; Chung KW; Choi BO Mol Med Rep; 2016 Jul; 14(1):33-40. PubMed ID: 27150940 [TBL] [Abstract][Full Text] [Related]
38. [Hereditary optic atrophies. Study of a family with dominant autosomal optic atrophy]. Sebastián de Erice M; Romero López J; Navarro Esteban J; Jiménez F; Soto Faure L Rev Clin Esp; 1981 Dec; 163(5):341-3. PubMed ID: 7342192 [No Abstract] [Full Text] [Related]
39. Hereditary motor and sensory neuropathy (proximal dominant form, HMSN-P) among Brazilians of Japanese ancestry. Maeda K; Sugiura M; Kato H; Sanada M; Kawai H; Yasuda H Clin Neurol Neurosurg; 2007 Nov; 109(9):830-2. PubMed ID: 17764830 [TBL] [Abstract][Full Text] [Related]
40. Familial spastic paraplegia with neuropathy and poikiloderma. A new syndrome? Antiñolo G; Nieto M; Borrego S; Sierra J; Rufo M; Siljeström ML Clin Genet; 1992 Jun; 41(6):281-4. PubMed ID: 1623621 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]