E. Al‐Sabban

发表

Infantile nephrotic syndrome and congenital glaucoma

M. Akhtar, J. Kari, S. Lingawi, 2001, Pediatric Nephrology.

Spectrum of glomerular disease among children in saudi arabia.

E. Al‐Sabban, 1997, Saudi journal of kidney diseases and transplantation : an official publication of the Saudi Center for Organ Transplantation, Saudi Arabia.

The Pitfall of White Blood Cell Cystine Measurement to Diagnose Juvenile Cystinosis

E. Levtchenko, S. Marie, K. Alsaad, 2023, International journal of molecular sciences.

Coxiella burnetii endocarditis in a child.

S. Al-Hajjar, S. Hussain Qadri, E. Al‐Sabban, 1997, The Pediatric infectious disease journal.

Clinical and epidemiological assessment of steroid-resistant nephrotic syndrome associated with the NPHS2 R229Q variant.

C. Antignac, L. Abel, J. Grünfeld, 2009, Kidney international.

A molecular genetic analysis of childhood nephrotic syndrome in a cohort of Saudi Arabian families

E. Faqeih, J. Sayer, B. Meyer, 2013, Journal of Human Genetics.

Paracellin-1, a renal tight junction protein required for paracellular Mg2+ resorption.

R. Lifton, S. Sanjad, D. Milford, 1999, Science.

Novel ATP6V1B1 and ATP6V0A4 mutations in autosomal recessive distal renal tubular acidosis with new evidence for hearing loss

S. Bianca, C. Morton, V. Tasic, 2002, Journal of medical genetics.

Novel ATP 6 V 1 B 1 and ATP 6 V 0 A 4 mutations in autosomal recessive distal renal tubular acidosis with new evidence for hearing loss

S. Bianca, C. Morton, V. Tasic, 2002 .

Gonadal mosaicism as a rare cause of autosomal recessive inheritance

S. Anazi, F. Alkuraya, E. Al-Sabban, 2014, Clinical genetics.

Mutations in ATP6N1B, encoding a new kidney vacuolar proton pump 116-kD subunit, cause recessive distal renal tubular acidosis with preserved hearing

S. Scherer, R. Lifton, A. Nayır, 2000, Nature Genetics.

A mutation in GLUT2, not in phosphorylase kinase subunits, in hepato-renal glycogenosis with Fanconi syndrome and low phosphorylase kinase activity.

B. Burwinkel, S. Sanjad, M. Kilimann, 1999 .

A mutation in GLUT2, not in phosphorylase kinase subunits, in hepato-renal glycogenosis with Fanconi syndrome and low phosphorylase kinase activity

B. Burwinkel, S. Sanjad, M. Kilimann, 1999, Human Genetics.

Kidney transplantations at King Faisal Specialist Hospital and Research Centre.

S. Sanjad, W. Qunibi, S. Taher, 1994, Annals of Saudi medicine.

Spectrum of Renal Disease in Saudi Arabia

S. Sanjad, W. Qunibi, S. Taher, 1990 .

Congenital chloride diarrhea: A single center experience with ten patients.

S. Sanjad, H. Nazer, A. Al-Abbad, 1995, Annals of Saudi medicine.

Localization of a gene for autosomal recessive distal renal tubular acidosis with normal hearing (rdRTA2) to 7q33-34.

R. Lifton, K. Finberg, A. Nayır, 1999, American journal of human genetics.

Hyperglycemia and Hypoinsulinemia in Patients with Fanconi-Bickel Syndrome

N. Al-Harbi, D. Taha, E. Al-Sabban, 2008, Journal of pediatric endocrinology & metabolism : JPEM.

Primary hyperoxaluria type 1: An underestimated cause of nephrocalcinosis and chronic renal failure in Saudi Arabian children.

S. Sanjad, A. Al-Abbad, E. Al‐Sabban, 1999, Annals of Saudi medicine.

Horseshoe kidney with hydronephrosis secondary to ureteric stenosis: construction of a ureter from the renal pelvis

S. Ahmed, E. Al‐Sabban, J. Abudaia, 1999, BJU international.

Renal transplantation associated with HIV infection : a Saudi Arabian experience and review of the literature

W. Qunibi, S. Taher, S. Bernvil, 1991 .

Post renal transplantation tubulopathies in children: a 9-year experience at a tertiary care centre.

A. Al-Abbad, E. Al-Sabban, A. Al-Ibrahim, 2004, Saudi journal of kidney diseases and transplantation : an official publication of the Saudi Center for Organ Transplantation, Saudi Arabia.

Coexistent Linear Scleroderma and Juvenile Systemic Lupus Erythematosus

S. Al‐Mayouf, S. Bahabri, E. Al-Sabban, 2000, Pediatric dermatology.

Clinical and epidemiological assessment of steroid-resistant nephrotic syndrome associated with the NPHS2 R229Q variant.

C. Antignac, L. Abel, J. Grünfeld, 2009, Kidney international.