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Sami Sanjad
Sami Sanjad
Professor of Pediatrics/Nephrology American University of Beirut Medical Center
Verified email at aub.edu.lb
Title
Cited by
Cited by
Year
Genetic diagnosis by whole exome capture and massively parallel DNA sequencing
M Choi, UI Scholl, W Ji, T Liu, IR Tikhonova, P Zumbo, A Nayir, ...
Proceedings of the National Academy of Sciences 106 (45), 19096-19101, 2009
18232009
Paracellin-1, a renal tight junction protein required for paracellular Mg2+ resorption
DB Simon, Y Lu, KA Choate, H Velazquez, E Al-Sabban, M Praga, ...
Science 285 (5424), 103-106, 1999
13341999
Bartter's syndrome, hypokalaemic alkalosis with hypercalciuria, is caused by mutations in the Na–K–2CI cotransporter NKCC2
DB Simon, FE Karet, JM Hamdan, AD Pietro, SA Sanjad, RP Lifton
Nature genetics 13 (2), 183-188, 1996
10861996
Mutations in the chloride channel gene, CLCNKB, cause Bartter's syndrome type III
DB Simon, RS Bindra, TA Mansfield, C Nelson-Williams, E Mendonca, ...
Nature genetics 17 (2), 171-178, 1997
10161997
Genetic heterogeneity of Barter's syndrome revealed by mutations in the K+ channel, ROMK
DB Simon, FE Karet, J Rodriguez-Soriano, JH Hamdan, A DiPietro, ...
Nature genetics 14 (2), 152-156, 1996
9561996
Mutations in the gene encoding B1 subunit of H+-ATPase cause renal tubular acidosis with sensorineural deafness
FE Karet, KE Finberg, RD Nelson, A Nayir, H Mocan, SA Sanjad, ...
Nature genetics 21 (1), 84-90, 1999
8141999
Mutations in kelch-like 3 and cullin 3 cause hypertension and electrolyte abnormalities
LM Boyden, M Choi, KA Choate, CJ Nelson-Williams, A Farhi, HR Toka, ...
Nature 482 (7383), 98-102, 2012
6512012
Mutations in ATP6N1B, encoding a new kidney vacuolar proton pump 116-kD subunit, cause recessive distal renal tubular acidosis with preserved hearing
AN Smith, J Skaug, KA Choate, A Nayir, A Bakkaloglu, S Ozen, SA Hulton, ...
Nature genetics 26 (1), 71-75, 2000
5202000
Novel ATP6V1B1 and ATP6V0A4 mutations in autosomal recessive distal renal tubular acidosis with new evidence for hearing loss
EH Stover, KJ Borthwick, C Bavalia, N Eady, DM Fritz, N Rungroj, ...
Journal of medical genetics 39 (11), 796-803, 2002
3642002
Idiopathic hypercalciuria: association with isolated hematuria and risk for urolithiasis in children
FB Stapleton, Southwest Pediatric Nephrology Study Group
Kidney Int 37 (2), 807-811, 1990
1921990
A new syndrome of congenital hypoparathyroidism, severe growth failure, and dysmorphic features.
SA Sanjad, NA Sakati, YK Abu-Osba, R Kaddoura, RD Milner
Archives of disease in childhood 66 (2), 193-196, 1991
1711991
Prognostic indicators in children with IgA nephropathy—report of the Southwest Pediatric Nephrology Study Group
RJ Hogg, FG Silva, RJ Wyatt, JS Reisch, J Craig Argyle, DA Savino
Pediatric nephrology 8, 15-20, 1994
1541994
Textbook of clinical pediatrics
AY Elzouki, HA Harfi, H Nazer, W Oh, FB Stapleton, RJ Whitley
Springer Science & Business Media, 2011
1332011
Localization of a gene for autosomal recessive distal renal tubular acidosis with normal hearing (rdRTA2) to 7q33-34
FE Karet, KE Finberg, A Nayir, A Bakkaloglu, S Ozen, SA Hulton, ...
The American Journal of Human Genetics 65 (6), 1656-1665, 1999
1181999
Management of hyperlipidemia in children with refractory nephrotic syndrome: the effect of statin therapy
SA Sanjad, A Al-Abbad, S Al-Shorafa
The Journal of pediatrics 130 (3), 470-474, 1997
901997
A clinico-pathologic study of crescentic glomerulonephritis in 50 children. A report of the Southwest Pediatric Nephrology Study Group
FW REISCH JS, S Centers
Kidney International 27, 450-8, 1985
841985
Nephropathy, an underestimated complication of methicillin therapy
SA Sanjad, GG Haddad, VH Nassar
The Journal of pediatrics 84 (6), 873-877, 1974
741974
Acute glomerulonephritis: A review of 153 cases.
Sanjad S, Tolimat A, Whitworth J, Levin S
Southern Medical Journal 70, 1202-1206, 1977
55*1977
Congenital hypoparathyroidism with dysmorphic features: a new syndrome
S Sanjad, N Sakati, Y Abu-Osba
Pediatr res 23 (3), 271A, 1988
541988
Confirmation of the assignment of the Sanjad-Sakati (congenital hypoparathyroidism) syndrome (OMIM 241410) locus to chromosome lq42-43
TE Kelly, S Blanton, R Saif, SA Sanjad, NA Sakati
Journal of Medical Genetics 37 (1), 63-64, 2000
452000
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