I. Lalani

Genetic aspects of amyotrophic lateral sclerosis.

T. Siddique, I. Lalani, 2002, Advances in neurology.

Emerging subspecialties in neurology: Pain medicine

I. Lalani, 2006, Neurology.

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

V. Mootha, S. Ajroud‐Driss, N. Siddique, 2014, neurogenetics.

Massive bleeding from angiomyolipoma of the kidney.

I. Lalani, 1977, Texas medicine.

Cranial nerve palsies in renal osteodystrophy.

J. Hunter, S. Facchini, A. Zakaria., 2007, Pediatric neurology.

Focal occipital seizures with cerebral polyopia.

A. Zakaria., I. Lalani, Laura Belorgey, 2006, Epileptic disorders : international epilepsy journal with videotape.

Phenotypic features and genetic findings in sacsin-related autosomal recessive ataxia in Tunisia.

W. Hung, T. Siddique, I. Turki, 2003, Archives of neurology.

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

V. Mootha, N. Siddique, T. Siddique, 2014, neurogenetics.

Interleukin-10: biology, role in inflammation and autoimmunity.

A. Ahmed, I. Lalani, K. Bhol, 1997, Annals of allergy, asthma & immunology : official publication of the American College of Allergy, Asthma, & Immunology.

Ischemic Stroke in the Setting of Tuberculous Meningitis

A. Zakaria., I. Lalani, Laura Belorgey, 2006, Journal of neuroimaging : official journal of the American Society of Neuroimaging.