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Authors: Ali G. Gharavi
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Journal Article

Heterozygous loss of WBP11 function causes multiple congenital defects in humans and mice Free

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Ella M M A Martin and others
Human Molecular Genetics, Volume 29, Issue 22, 15 November 2020, Pages 3662–3678, https://doi.org/10.1093/hmg/ddaa258
Published: 04 December 2020
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A 5-year survey of biopsy proven kidney diseases in Lebanon: significant variation in prevalence of primary glomerular diseases by age, population structure and consanguinity Get access

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Hussein H. Karnib and others
Nephrology Dialysis Transplantation, Volume 25, Issue 12, December 2010, Pages 3962–3969, https://doi.org/10.1093/ndt/gfq302
Published: 04 June 2010
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IgA nephropathy—the case for a genetic basis becomes stronger Get access

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Krzysztof Kiryluk and others
Nephrology Dialysis Transplantation, Volume 25, Issue 2, February 2010, Pages 336–338, https://doi.org/10.1093/ndt/gfp593
Published: 13 November 2009
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Characterization of a large Lebanese family segregating IgA nephropathy Get access

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Hussein H. Karnib and others
Nephrology Dialysis Transplantation, Volume 22, Issue 3, March 2007, Pages 772–777, https://doi.org/10.1093/ndt/gfl677
Published: 15 December 2006
Journal Article

Resting Diastolic Function and Left Ventricular Mass are Related to Exercise Capacity in Hypertensive Men but not in Women Get access

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Ali G. Gharavi and others
American Journal of Hypertension, Volume 11, Issue 10, October 1998, Pages 1252–1257, https://doi.org/10.1016/S0895-7061(98)00138-1
Published: 01 October 1998
Journal Article

Ambulatory Blood Pressure Monitoring for Detecting the Relation Between Angiotensinogen Gene Polymorphism and Hypertension Get access

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Ali G. Gharavi and others
American Journal of Hypertension, Volume 10, Issue 6, June 1997, Pages 687–691, https://doi.org/10.1016/S0895-7061(97)00097-6
Published: 01 June 1997