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Dihydropyridine receptor mutations cause hypokalemic periodic paralysis.

• Louis J. Ptácek, Rami Tawil, +7 authors Gameil T. Fouad
• Cell
• 1994

Hypokalemic periodic paralysis (hypoKPP) is an autosomal dominant skeletal muscle disorder manifested by episodic weakness associated with low serum potassium. Genetic linkage analysis has localized… (More)

Genotype-phenotype correlations of DHP receptor alpha 1-subunit gene mutations causing hypokalemic periodic paralysis.

• Gameil T. Fouad, Marinos C. Dalakas, +12 authors Louis J. Ptácek
• Neuromuscular disorders : NMD
• 1997

Hypokalemic periodic paralysis (hypoKPP) is an autosomal dominant or sporadic disorder characterized by periodic, reversible attacks of muscle weakness. Mutations in the skeletal muscle… (More)

Penile prosthesis surgery under local penile block anaesthesia via the infrapubic space.

• Hussein M Ghanem, Gameil T. Fouad
• International journal of andrology
• 2000

The aim of this study was to evaluate the effectiveness and patient tolerance to local penile block anaesthesia via the infrapubic space with penile prosthesis implantation. Local anaesthesia was… (More)

Allelic Interaction between CRELD1 and VEGFA in the Pathogenesis of Cardiac Atrioventricular Septal Defects

• Jennifer K. Redig, Gameil T. Fouad, +4 authors Cheryl L Maslen
• AIMS genetics
• 2014

Atrioventricular septal defects (AVSD) are highly heritable, clinically significant congenital heart malformations. Genetic and environmental modifiers of risk are thought to work in unknown… (More)

A randomized, double-blind clinical study on the safety and tolerability of an iron multi-amino acid chelate preparation in premenopausal women.

• Gameil T. Fouad, Malkanthi Evans, Prachi Sharma, Joshua E Baisley, David Crowley, Najla Guthrie
• Journal of dietary supplements
• 2013

ABSTRACT Considerable risk of iron deficiency has been identified in premenopausal women because of the adverse effects associated with commercial iron preparations. This study examined the safety… (More)

Identification, genomic organization and mRNA expression of CRELD1, the founding member of a unique family of matricellular proteins.

• Paul A. Rupp, Gameil T. Fouad, +7 authors Cheryl L Maslen
• Gene
• 2002

We have isolated and characterized a unique gene that encodes a highly conserved membrane bound extracellular protein that defines a new epidermal growth factor-related gene family. The CRELD1… (More)

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