Kutai M - Search Results

1

Clinical characteristics and muscle pathology in myopathic mitochondrial DNA depletion.

Nevo Y, Soffer D, Kutai M, Zelnik N, Saada A, Jossiphov J, Messer G, Shaag A, Shahar E, Harel S, Elpeleg O. Nevo Y, et al. Among authors: kutai m. J Child Neurol. 2002 Jul;17(7):499-504. doi: 10.1177/088307380201700705. J Child Neurol. 2002. PMID: 12269728

2

Congenital muscular dystrophy in Israeli families.

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

3

Childhood macrophagic myofasciitis-consanguinity and clinicopathological features.

Nevo Y, Kutai M, Jossiphov J, Livne A, Neeman Z, Arad T, Popovitz-Biro R, Atsmon J, Shapira Y, Soffer D. Nevo Y, et al. Among authors: kutai m. Neuromuscul Disord. 2004 Apr;14(4):246-52. doi: 10.1016/j.nmd.2003.12.005. Neuromuscul Disord. 2004. PMID: 15019702

4

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: kutai m. J Child Neurol. 2007 Jun;22(6):732-6. doi: 10.1177/0883073807304193. J Child Neurol. 2007. PMID: 17641259

5

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. Among authors: kutai m. Isr Med Assoc J. 2003 Feb;5(2):94-7. Isr Med Assoc J. 2003. PMID: 12674656 Free article.

6

Unprovoked seizures and developmental disabilities: clinical characteristics of children referred to a child development center.

Nevo Y, Shinnar S, Samuel E, Kramer U, Leitner Y, Fatal A, Kutai M, Harel S. Nevo Y, et al. Among authors: kutai m. Pediatr Neurol. 1995 Oct;13(3):235-41. doi: 10.1016/0887-8994(95)00185-i. Pediatr Neurol. 1995. PMID: 8554661

7

Clinical characteristics of children referred to a child development center for evaluation of speech, language, and communication disorders.

Harel S, Greenstein Y, Kramer U, Yifat R, Samuel E, Nevo Y, Leitner Y, Kutai M, Fattal A, Shinnar S. Harel S, et al. Among authors: kutai m. Pediatr Neurol. 1996 Nov;15(4):305-11. doi: 10.1016/s0887-8994(96)00222-6. Pediatr Neurol. 1996. PMID: 8972529

8

Neurodevelopmental outcome in children with intrauterine growth retardation: a 3-year follow-up.

Fattal-Valevski A, Leitner Y, Kutai M, Tal-Posener E, Tomer A, Lieberman D, Jaffa A, Many A, Harel S. Fattal-Valevski A, et al. Among authors: kutai m. J Child Neurol. 1999 Nov;14(11):724-7. doi: 10.1177/088307389901401107. J Child Neurol. 1999. PMID: 10593549

9

Six-year follow-up of children with intrauterine growth retardation: long-term, prospective study.

Leitner Y, Fattal-Valevski A, Geva R, Bassan H, Posner E, Kutai M, Many A, Jaffa AJ, Harel S. Leitner Y, et al. Among authors: kutai m. J Child Neurol. 2000 Dec;15(12):781-6. doi: 10.1177/088307380001501202. J Child Neurol. 2000. PMID: 11198491

10

Hereditary hypotonia, muscle weakness, failure to thrive, and cognitive delay in a large moslem kindred.

Kutai M, Shalev SA, Chervinski I, Mazor G, Rabie M, Nevo Y. Kutai M, et al. Pediatr Neurol. 2006 Dec;35(6):425-9. doi: 10.1016/j.pediatrneurol.2006.06.017. Pediatr Neurol. 2006. PMID: 17138013

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