Nevo Y - Search Results

1

Novel mutations in the emerin gene in Israeli families.

Nevo Y, Ahituv S, Yaron Y, Kedmi M, Shomrat R, Legum C, Orr-Urtreger A. Nevo Y, et al. Hum Mutat. 2001 Jun;17(6):522. doi: 10.1002/humu.1139. Hum Mutat. 2001. PMID: 11385714

2

SMA type 2 unrelated to chromosome 5q13.

Nevo Y, Kramer U, Legum C, Shomrat R, Fatal A, Soffer D, Harel S, Shapira Y. Nevo Y, et al. Am J Med Genet. 1998 Jan 13;75(2):193-5. Am J Med Genet. 1998. PMID: 9450884

3

Fetal muscle biopsy as a diagnostic tool in Duchenne muscular dystrophy.

Nevo Y, Shomrat R, Yaron Y, Orr-Urtreger A, Harel S, Legum C. Nevo Y, et al. Prenat Diagn. 1999 Oct;19(10):921-6. doi: 10.1002/(sici)1097-0223(199910)19:10<921::aid-pd660>3.0.co;2-a. Prenat Diagn. 1999. PMID: 10521816

4

A case of Bartter's syndrome, gout and Becker's muscular dystrophy.

Fishel B, Zhukovsky G, Legum C, Jossiphov J, Alon M, Peer G, Iaina A, Nevo Y. Fishel B, et al. Among authors: nevo y. Clin Exp Rheumatol. 2000 May-Jun;18(3):426-7. Clin Exp Rheumatol. 2000. PMID: 10895394 No abstract available.

5

[Update on diagnosis of limb girdle muscular dystrophy].

Nevo Y, Yaron Y. Nevo Y, et al. Harefuah. 1999 May 2;136(9):720-5. Harefuah. 1999. PMID: 10955098 Review. Hebrew. No abstract available.

6

Large in-frame deletions of the rod-shaped domain of the dystrophin gene resulting in severe phenotype.

Nevo Y, Muntoni F, Sewry C, Legum C, Kutai M, Harel S, Dubowitz V. Nevo Y, et al. Isr Med Assoc J. 2003 Feb;5(2):94-7. Isr Med Assoc J. 2003. PMID: 12674656 Free article.

7

Congenital myopathies in Israeli families.

Weiss K, Shapira Y, Glick B, Lerman-Sagie T, Shahar E, Goez H, Kutai M, Nevo Y. Weiss K, et al. Among authors: nevo y. J Child Neurol. 2007 Jun;22(6):732-6. doi: 10.1177/0883073807304193. J Child Neurol. 2007. PMID: 17641259

8

Congenital muscular dystrophy in Israeli families.

Rachmiel M, Nevo Y, Lahat E, Kutai M, Harel S, Shahar E. Rachmiel M, et al. Among authors: nevo y. J Child Neurol. 2002 May;17(5):333-6. doi: 10.1177/088307380201700504. J Child Neurol. 2002. PMID: 12150578

9

Pax7, Pax3 and Mamstr genes are involved in skeletal muscle impaired regeneration of dy2J/dy2J mouse model of Lama2-CMD.

Yanay N, Elbaz M, Konikov-Rozenman J, Elgavish S, Nevo Y, Fellig Y, Rabie M, Mitrani-Rosenbaum S, Nevo Y. Yanay N, et al. Among authors: nevo y. Hum Mol Genet. 2019 Oct 15;28(20):3369-3390. doi: 10.1093/hmg/ddz180. Hum Mol Genet. 2019. PMID: 31348492

10

Mutation analysis in Emery-Dreifuss muscular dystrophy.

Nevo Y, Al-Lozi M, Parsadanian AS, Elliott JL, Connolly AM, Pestronk A. Nevo Y, et al. Pediatr Neurol. 1999 Jul;21(1):456-9. doi: 10.1016/s0887-8994(99)00023-5. Pediatr Neurol. 1999. PMID: 10428430

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