Naffaa Al-Harbi

Next-generation sequencing for molecular diagnosis of autosomal recessive polycystic kidney disease.

M. Athar, F. Al-Allaf, M. Taher, 2016, Gene.

A molecular genetic analysis of childhood nephrotic syndrome in a cohort of Saudi Arabian families

E. Faqeih, J. Sayer, B. Meyer, 2013, Journal of Human Genetics.

Functional alterations due to amino acid changes and evolutionary comparative analysis of ARPKD and ADPKD genes

M. Athar, F. Al-Allaf, M. Taher, 2016, Genomics data.

Hyperglycemia and Hypoinsulinemia in Patients with Fanconi-Bickel Syndrome

N. Al-Harbi, D. Taha, E. Al-Sabban, 2008, Journal of pediatric endocrinology & metabolism : JPEM.

Hypocalcemia and Hypomagnesemia after Ibuprofen Overdose

S. Domrongkitchaiporn, D. Lirenman, Naffaa Al-Harbi, 1997, The Annals of pharmacotherapy.

Arthrogryposis, renal tubular acidosis and cholestasis (ARC) syndrome: two new cases and review

D. Taha, M. Barbar, Omar Abu-Sa’da, 2005, Clinical dysmorphology.

Congenital Insensitivity to Pain in Four Related Saudi Families

Naffaa Al-Harbi, Eman M. Karkashan, Hanan S. Joharji, 2002, Pediatric dermatology.