Miladi N - Search Results

1

[Primary immunodeficiency in Tunisia: study of 152 cases].

Bejaoui M, Barbouche MR, Sassi A, Larguche B, Miladi N, Bouguerra A, Dellagi K. Bejaoui M, et al. Among authors: miladi n. Arch Pediatr. 1997 Sep;4(9):827-31. doi: 10.1016/s0929-693x(97)88145-6. Arch Pediatr. 1997. PMID: 9345562 French.

2

[Strabismus, nystagmus, and generalized hypotonia in a 7-month-old child].

Nagi S, Brahim I, Hammami N, Drissi C, Ben Ammou B, Miladi N, Ben Hamouda M. Nagi S, et al. Among authors: miladi n. Arch Pediatr. 2012 Jan;19(1):62-3, 74-6. doi: 10.1016/j.arcped.2011.10.014. Epub 2011 Nov 29. Arch Pediatr. 2012. PMID: 22130616 French. No abstract available.

3

Duchenne muscular dystrophy in Tunisia: a clinical and morphological study of 77 cases.

Ben Hamida M, Miladi N, Turki I, Zaiem H. Ben Hamida M, et al. Among authors: miladi n. J Neurol Sci. 1992 Jan;107(1):60-4. doi: 10.1016/0022-510x(92)90209-4. J Neurol Sci. 1992. PMID: 1578235

4

[Genetic study of spinocerebellar hereditary degenerations in Tunisia. Role of consanguinity in their occurrence].

Ben Hamida M, Chaabouni H, Madani S, Boussen S, Samoud S, Letaief F, Mrabet A, Hentati F, Miladi N. Ben Hamida M, et al. Among authors: miladi n. J Genet Hum. 1986 Aug;34(3-4):267-74. J Genet Hum. 1986. PMID: 3760830 French.

5

Dihydropteridine reductase deficiency in a large consanguineous Tunisian family: clinical, biochemical, and neuropathologic findings.

Miladi N, Larnaout A, Dhondt JL, Vincent MF, Kaabachi N, Hentati F. Miladi N, et al. J Child Neurol. 1998 Oct;13(10):475-80. doi: 10.1177/088307389801301002. J Child Neurol. 1998. PMID: 9796752

6

Phenotypic spectrum of fucosidosis in Tunisia.

Ben Turkia H, Tebib N, Azzouz H, Abdelmoula MS, Bouguila J, Sanhaji H, Miladi N, Maire I, Caillaud C, Kaabachi N, Ben Dridi MF. Ben Turkia H, et al. Among authors: miladi n. J Inherit Metab Dis. 2008 Dec;31 Suppl 2:S313-6. doi: 10.1007/s10545-008-0891-0. Epub 2008 Jul 27. J Inherit Metab Dis. 2008. PMID: 18651239

7

[Schwartz-Jampel syndrome. Clinical and histopathological study of 4 cases].

Ben Hamida M, Miladi N, Ben Hamida C. Ben Hamida M, et al. Among authors: miladi n. Rev Neurol (Paris). 1991;147(4):279-84. Rev Neurol (Paris). 1991. PMID: 2063077 Review. French.

8

[How to treat epilepsy in children?].

Miladi N, Larnaout A, Turki I. Miladi N, et al. Tunis Med. 1992 Jun-Jul;70(6-7):325-7. Tunis Med. 1992. PMID: 1448855 Review. French. No abstract available.

9

Phenylketonuria: an underlying etiology of autistic syndrome. A case report.

Miladi N, Larnaout A, Kaabachi N, Helayem M, Ben Hamida M. Miladi N, et al. J Child Neurol. 1992 Jan;7(1):22-3. doi: 10.1177/088307389200700103. J Child Neurol. 1992. PMID: 1552146

10

[Continence disorders in hereditary spinocerebellar degeneration. Comparison of clinical and urodynamic findings in 55 cases].

Chami I, Miladi N, Ben Hamida M, Zmerli S. Chami I, et al. Among authors: miladi n. Acta Neurol Belg. 1984 Aug-Oct;84(4):194-203. Acta Neurol Belg. 1984. PMID: 6496033 French.

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