M. Salih

Autosomal-recessive forms of demyelinating Charcot-Marie-Tooth disease

M. Ruberg, A. Brice, N. Birouk, 2007, NeuroMolecular Medicine.

Autosomal recessive hereditary neuropathy with focally folded myelin sheaths and linked to chromosome 11q23: a distinct and homogeneous entity

A. Brice, T. Maisonobe, D. Grid, 2000, Neuromuscular Disorders.

Chlamydial etiology of acute lower respiratory tract infections in children in the Sudan

P. Mårdh, B. Herrmann, B. Yousif, 1994, Acta paediatrica.

Clinical, biochemical and molecular characterization of peroxisomal diseases in Arabs

N. Shimozawa, R. Shaheen, M. Hashem, 2011, Clinical genetics.

CLINICAL AND MOLECULAR PATHOLOGICAL FEATURES OF SEVERE CHILDHOOD AUTOSOMAL RECESSIVE MUSCULAR DYSTROPHY IN SAUDI ARABIA

K. Campbell, S. Roberds, M. Salih, 1996, Developmental medicine and child neurology.

Plasma fatty acid abnormality in Sudanese drug-resistant epileptic patients.

M. I. Elbashir, I. Mohamed, K. Ghebremeskel, 2021, Prostaglandins, leukotrienes, and essential fatty acids.