Irfan Lalani

Mutation in the novel nuclear-encoded mitochondrial protein CHCHD10 in a family with autosomal dominant mitochondrial myopathy

Senda Ajroud‐Driss, Faisal Fecto, Kaouther Ajroud et al. · Neurogenetics · 2014 · 126 citations · Full text

Mitochondrial Myopathy, Mendelian Disorder, Mitochondrial Function +6

Phenotypic Features and Genetic Findings in Sacsin-Related Autosomal Recessive Ataxia in Tunisia

Ghada El Euch-Fayache, Irfan Lalani, Rim Amouri et al. · Archives of Neurology · 2003 · 107 citations

Cranial Nerve Palsies in Renal Osteodystrophy

Farida Abid, Irfan Lalani, Asma Zakaria et al. · Pediatric Neurology · 2006 · 35 citations

Axial Skeleton, Urology, Cranial Nerve Palsies +8

Genetic aspects of amyotrophic lateral sclerosis.

Teepu Siddique, Irfan Lalani · PubMed · 2002 · 25 citations

Neurodegenerative Diseases, Amyotrophic Lateral Sclerosis, Neurological Disorder +5

Aspiration pneumonia in pediatric age group: etiology, predisposing factors and clinical outcome.

Rezaul Karim, I. A. Momin, Irfan Lalani et al. · PubMed · 1999 · 18 citations