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Sami Sanjad

Research Profile

Concepts & Ideas

Physiology

Genes & Molecular Sequences

Living Beings

Disorders

Chemicals & Drugs

Procedures

Kidney Transplantation

Phenomena

Polymorphism, Single-Stranded Conformational

Co-author Network

Publications

TOP 3
Sami A Sanjad
Etiology of hypertension in children and adolescents.
Murim Choi; Ute I Scholl; Weizhen Ji; Tiewen Liu; Irina R Tikhonova; Paul Zumbo; AHMET NAYIR; Ayşin Bakkaloğlu; Seza Ozen; Sami A Sanjad; Carol Nelson-Williams; anita farhi; Shrikant M Mane; Richard P Lifton
Genetic diagnosis by whole exome capture and massively parallel DNA sequencing.
Samar A Muwakkit; Raya Saab; Sami A Sanjad; Saleh I Bhar; Rim S Ishak; Zeina A Samad; Anthony K Chan; Miguel R Abboud
Renal venous thrombosis in a newborn with prothrombotic risk factors.

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All Publications

2010: Sami A Sanjad
Etiology of hypertension in children and adolescents.
Le Journal médical libanais. The Lebanese medical journal 2010;58(3):142-5.
2009: Murim Choi; Ute I Scholl; Weizhen Ji; Tiewen Liu; Irina R Tikhonova; Paul Zumbo; AHMET NAYIR; Ayşin Bakkaloğlu; Seza Ozen; Sami A Sanjad; Carol Nelson-Williams; anita farhi; Shrikant M Mane; Richard P Lifton
Genetic diagnosis by whole exome capture and massively parallel DNA sequencing.
Proceedings of the National Academy of Sciences of the United States of America 2009;106(45):19096-101.
2009: Samar A Muwakkit; Raya Saab; Sami A Sanjad; Saleh I Bhar; Rim S Ishak; Zeina A Samad; Anthony K Chan; Miguel R Abboud
Renal venous thrombosis in a newborn with prothrombotic risk factors.
Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis 2009;20(6):458-60.
2007: Sami A Sanjad; Ali Hariri; Zuheir Habbal; Richard P Lifton
A novel PCLN-1 gene mutation in familial hypomagnesemia with hypercalciuria and atypical phenotype.
Pediatric nephrology (Berlin, Germany) 2007;22(4):503-8.
2003: Sami A Sanjad
Renal tubular acidosis in the arab world.
Saudi journal of kidney diseases and transplantation : an official publication of the Saudi Center for Organ Transplantation, Saudi Arabia 2003;14(3):305-13.
2001: Sami A Sanjad; A Ibrahim; S Al Shorafa; ABBAS ALABBAD; R B Khauli; K A Shaibani; EA al-Sabban
Renal tubular dysfunction following kidney transplantation: a prospective study in 31 children.
Transplantation proceedings 2001;33(5):2830-1.
2001: Raja B Khauli; Walid Medawar; AA Habbal; A E Birbari; MM Daouk; Alexander M Abdelnoor; Marwan Uwaydah; A Rahman Bizri; Sami A Sanjad; P J Ayvazian; TD Lovewell; Jeffrey S Stoff; P Yang Fan; P Bigwood; robert harland
Improved primary transplant success rates using a triple regimen of cyclosporine microemulsion, mycophenolate mofetil and prednisone.
Transplantation proceedings 2001;33(5):2776-7.
2000: Annabel N Smith; J Skaug; Keith Choate; AHMET NAYIR; A Bakkaloglu; S Ozen; SA Hulton; Sami A Sanjad; EA al-Sabban; Richard P Lifton; S W Scherer; Fiona E Karet
Mutations in ATP6N1B, encoding a new kidney vacuolar proton pump 116-kD subunit, cause recessive distal renal tubular acidosis with preserved hearing.
Nature genetics 2000;26(1):71-5.
1999: Fiona E Karet; Karin E Finberg; AHMET NAYIR; A Bakkaloglu; S Ozen; SA Hulton; Sami A Sanjad; EA al-Sabban; J F Medina; Richard P Lifton
Localization of a gene for autosomal recessive distal renal tubular acidosis with normal hearing (rdRTA2) to 7q33-34.
American journal of human genetics 1999;65(6):1656-65.
1999: Barbara Burwinkel; Sami A Sanjad; EA al-Sabban; ABBAS ALABBAD; Manfred W Kilimann
A mutation in GLUT2, not in phosphorylase kinase subunits, in hepato-renal glycogenosis with Fanconi syndrome and low phosphorylase kinase activity.
Human genetics 1999;105(3):240-3.
1999: DB Simon; Y Lu; Keith Choate; Heino Velazquez; EA al-Sabban; M Praga; G Casari; Alberto Bettinelli; Giacomo Colussi; Juan Rodriguez Soriano; D McCredie; D Milford; Sami A Sanjad; Richard P Lifton
Paracellin-1, a renal tight junction protein required for paracellular Mg2+ resorption.
Science (New York, N.Y.) 1999;285(5424):103-6.
1999: George A Diaz; Bruce D Gelb; F Ali; Nadia A Sakati; Sami A Sanjad; Brian F Meyer; Marios Kambouris
Sanjad-Sakati and autosomal recessive Kenny-Caffey syndromes are allelic: evidence for an ancestral founder mutation and locus refinement.
American journal of medical genetics 1999;85(1):48-52.
1999: Emtethal Al-Jishi; Brian F Meyer; Mohamed S Rashed; Mazen Al-Essa; Mohamed Al-Hamed; Nadia A Sakati; Sami A Sanjad; Pinar T Ozand; Marios Kambouris
Clinical, biochemical, and molecular characterization of patients with glutathione synthetase deficiency.
Clinical genetics 1999;55(6):444-9.
1999: Sami A Sanjad; ABBAS ALABBAD; EA al-Sabban
Primary hyperoxaluria type 1: An underestimated cause of nephrocalcinosis and chronic renal failure in Saudi Arabian children.
Annals of Saudi medicine 1999;19(1):4-7.
1999: Fiona E Karet; Karin E Finberg; R D Nelson; AHMET NAYIR; H Mocan; Sami A Sanjad; Juan Rodriguez Soriano; F Santos; C W Cremers; A Di Pietro; B I Hoffbrand; J Winiarski; A Bakkaloglu; S Ozen; R Dusunsel; P Goodyer; SA Hulton; D K Wu; A B Skvorak; C C Morton; M J Cunningham; V Jha; Richard P Lifton
Mutations in the gene encoding B1 subunit of H+-ATPase cause renal tubular acidosis with sensorineural deafness.
Nature genetics 1999;21(1):84-90.
1997: DB Simon; Ranjit Bindra; T A Mansfield; Carol Nelson-Williams; E Mendonca; R Stone; S Schurman; AHMET NAYIR; H Alpay; A Bakkaloglu; Juan Rodriguez Soriano; J M Morales; Sami A Sanjad; C M Taylor; D Pilz; A Brem; Howard Trachtman; W Griswold; G A Richard; E John; Richard P Lifton
Mutations in the chloride channel gene, CLCNKB, cause Bartter's syndrome type III.
Nature genetics 1997;17(2):171-8.
1997: Sami A Sanjad
Hereditary and acquired renal tubular disorders: the saudi experience.
Saudi journal of kidney diseases and transplantation : an official publication of the Saudi Center for Organ Transplantation, Saudi Arabia 1997;8(3):247-59.
1997: Sami A Sanjad; ABBAS ALABBAD; S al-Shorafa
Management of hyperlipidemia in children with refractory nephrotic syndrome: the effect of statin therapy.
The Journal of pediatrics 1997;130(3):470-4.
1996: DB Simon; Fiona E Karet; Juan Rodriguez Soriano; J H Hamdan; A DiPietro; Howard Trachtman; Sami A Sanjad; R P Lifton
Genetic heterogeneity of Bartter's syndrome revealed by mutations in the K+ channel, ROMK.
Nature genetics 1996;14(2):152-6.
1996: DB Simon; Fiona E Karet; J M Hamdan; A DiPietro; Sami A Sanjad; R P Lifton
Bartter's syndrome, hypokalaemic alkalosis with hypercalciuria, is caused by mutations in the Na-K-2Cl cotransporter NKCC2.
Nature genetics 1996;13(2):183-8.
1994: G Lundgren; O Al-Furayh; Mohammed Akhtar; Y Barri; H Collste; Khalid Al Meshari; Wajeh Y Qunibi; EA al-Sabban; Sami A Sanjad; Khalid Al Shaibani; K Sheth; S Taher
Kidney transplantations at King Faisal Specialist Hospital and Research Centre.
Annals of Saudi medicine 1994;14(1):5-11.
1993: Sami A Sanjad; R E Kaddoura; H M Nazer; M Akhtar; Nadia A Sakati
Fanconi's syndrome with hepatorenal glycogenosis associated with phosphorylase b kinase deficiency.
American journal of diseases of children (1960) 1993;147(9):957-9.
1992: G Lundgren; Osman A Alfurayh; B B Duffy; P Nicholls; Wajeh Y Qunibi; EA al-Sabban; Sami A Sanjad; S Taher
Five-years' experience with cadaveric kidney transplantation at King Faisal Specialist Hospital and Research Center, Riyadh.
Transplantation proceedings 1992;24(5):1840.
1992: G Lundgren; Osman A Alfurayh; C Collste; B B Duffy; P Nicholls; EA al-Sabban; Sami A Sanjad; S Taher; Wajeh Y Qunibi
The kidney transplantation program at King Faisal Specialist Hospital and Research Centre, Riyadh.
Transplantation proceedings 1992;24(1):336-8.
1991: Sami A Sanjad; Nadia A Sakati; Y K Abu-Osba; R Kaddoura; R D Milner
A new syndrome of congenital hypoparathyroidism, severe growth failure, and dysmorphic features.
Archives of disease in childhood 1991;66(2):193-6.