Amar Al-Shibli

Renal tract abnormalities missed in a historical cohort of young children with UTI if the NICE and AAP imaging guidelines were applied

Hassib Narchı, Muhaned A. Marah, Asad Aziz Khan et al. · Journal of Pediatric Urology · 2015 · 32 citations

Urogenital Radiology, Urology, Medicine +11

Familial hypomagnesemia with hypercalciuria and nephrocalcinosis (FHHNC): Report of three cases with a novel mutation in CLDN19 gene

Amar Al-Shibli, Martin Konrad, Waleed Altay et al. · Saudi Journal of Kidney Diseases and Transplantation · 2013 · 19 citations · Full text

Novel DNA mutation in the GATA3 gene in an Emirati boy with HDR syndrome and hypomagnesemia

Amar Al-Shibli, Ibrahim Al Attrach, Patrick J. Willems · Pediatric Nephrology · 2011 · 19 citations

Novel Dna Mutation, Mendelian Disorder, Hdr Syndrome +10

Mixed Bartter-Gitelman syndrome: an inbred family with a heterogeneous phenotype expression of a novel variant in the CLCNKB gene

Amar Al-Shibli, Madinah Yusuf, Issam Abounajab et al. · SpringerPlus · 2014 · 15 citations · Full text

Novel Missense Variant, Genetics, Renal Pathology +18