Naffaa Al-Harbi - Concepedia

Author

Naffaa Al-Harbi

King Faisal Specialist Hospital & Research Centre

Also Known As

Naffaa Al-Harbi, Naffaa Alharbi, Naffaa N Al-Harbi, Naffaa N. Al‐Harbi

Publications

206

Citations

H-Index

Concepts

All Affiliations

King Faisal Specialist Hospital & Research Centre King Fahd Medical City Armed Forces Hospital King Abdullah Medical City King Saud University

About

Naffaa Al-Harbi is an author at King Faisal Specialist Hospital & Research Centre specializing in medicine, chronic kidney disease, and nephrology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	4	4	112
2	Nephrology	3	3	96
3	Biochemistry	1	1	16
4	Molecular Medicine	1	1	16
5	Neurology	1	1	26

Naffaa Al-Harbi

Publications

201

Citations

H-Index

Page 1

	Year	Citations
A molecular genetic analysis of childhood nephrotic syndrome in a cohort of Saudi Arabian families Mohamed H. Al‐Hamed, Essam Al‐Sabban, Hamad Al‐Mojalli, Journal of Human Genetics GlomerulonephritisGenetic DisorderMedicineGeneticsInherited Metabolic Disease	2013	50
Hyperglycemia and Hypoinsulinemia in Patients with Fanconi-Bickel Syndrome Doris Taha, Naffaa Al-Harbi, Essam Al‐Sabban Journal of Pediatric Endocrinology and Metabolism	2008	37
Arthrogryposis, renal tubular acidosis and cholestasis (ARC) syndrome: two new cases and review Omar Abu-Sa da, Maha Barbar, Naffaa Al-Harbi, Clinical Dysmorphology GlomerulonephritisArc SyndromeUrologyClinical FindingSaudi Infants	2005	26
Hypocalcemia and Hypomagnesemia after Ibuprofen Overdose Naffaa Al-Harbi, Somnuek Domrongkitchaiporn, David S. Lirenman Annals of Pharmacotherapy	1997	24
Next-generation sequencing for molecular diagnosis of autosomal recessive polycystic kidney disease Burhan Edrees, Mohammad Athar, Faisal A. Al-Allaf, Gene Molecular DiagnosisUrologyMendelian DisorderMedicineGenetics	2016	20
Congenital Insensitivity to Pain in Four Related Saudi Families Eman M. Karkashan, Hanan Joharji, Naffaa Al-Harbi Pediatric Dermatology	2002	18
Apparent Mineralocorticoid Excess Caused by a Novel Mutation in 11-β Hydroxysteroid Dehydrogenase type 2 Enzyme: its Genetics and Response to Therapy Ali S. Alzahrani, Nasser Aljuhani, Ebtesam Qasem, Endocrine Practice Novel MutationBiochemistryApparent Mineralocorticoid ExcessGeneticsPathology	2014	16
Functional alterations due to amino acid changes and evolutionary comparative analysis of ARPKD and ADPKD genes Burhan Edrees, Mohammad Athar, Zainularifeen Abduljaleel, Genomics Data	2016	10

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