A molecular genetic analysis of childhood nephrotic syndrome in a cohort of Saudi Arabian families von Al-Hamed, Mohamed H, Al-Sabban, Essam, Al-Mojalli, Hamad, Al-Harbi, Naffaa, Faqeih, Eissa, Al Shaya, Hammad, Alhasan, Khalid, Al-Hissi, Safaa, Rajab, Mohamed, Edwards, Noel, Al-Abbad, Abbas, Al-Hassoun, Ibrahim, Sayer, John A, Meyer, Brian F

Volltext

The morbid genome of ciliopathies: an update von Shamseldin, Hanan E., Shaheen, Ranad, Ewida, Nour, Bubshait, Dalal K., Alkuraya, Hisham, Almardawi, Elham, Howaidi, Ali, Sabr, Yasser, Abdalla, Ebtesam M., Alfaifi, Abdullah Y., Alghamdi, Jameel Mohammed, Alsagheir, Afaf, Alfares, Ahmed, Morsy, Heba, Hussein, Maged H., Al–Muhaizea, Mohammad A., Shagrani, Mohammad, Al Sabban, Essam, Salih, Mustafa A., Meriki, Neama, Khan, Rubina, Almugbel, Maisoon, Qari, Alya, Tulba, Maha, Mahnashi, Mohammed, Alhazmi, Khalid, Alsalamah, Abrar K., Nowilaty, Sawsan R., Alhashem, Amal, Hashem, Mais, Abdulwahab, Firdous, Ibrahim, Niema, Alshidi, Tarfa, AlObeid, Eman, Alenazi, Mona M., Alzaidan, Hamad, Rahbeeni, Zuhair, Al–Owain, Mohammed, Sogaty, Sameera, Seidahmed, Mohammed Zain, Alkuraya, Fowzan S.

Volltext

Type IV Collagen Mutations in Familial IgA Nephropathy von Li, Yifu, Groopman, Emily E., D’Agati, Vivette, Prakash, Sindhuri, Zhang, Junying, Mizerska-Wasiak, Malgorzata, Caliskan, Yasar, Fasel, David, Karnib, Hussein H., Bono, Luisa, Omran, Sadek Al, Sabban, Essam Al, Kiryluk, Krzysztof, Caridi, Gianluca, Ghiggeri, Gian Marco, Sanna-Cherchi, Simone, Scolari, Francesco, Gharavi, Ali G.

Volltext

The morbid genome of ciliopathies: an update von Shamseldin, Hanan E., Shaheen, Ranad, Ewida, Nour, Bubshait, Dalal K., Alkuraya, Hisham, Almardawi, Elham, Howaidi, Ali, Sabr, Yasser, Abdalla, Ebtesam M., Alfaifi, Abdullah Y., Alghamdi, Jameel Mohammed, Alsagheir, Afaf, Alfares, Ahmed, Morsy, Heba, Hussein, Maged H., Al–Muhaizea, Mohammad A., Shagrani, Mohammad, Al Sabban, Essam, Salih, Mustafa A., Meriki, Neama, Khan, Rubina, Almugbel, Maisoon, Qari, Alya, Tulba, Maha, Mahnashi, Mohammed, Alhazmi, Khalid, Alsalamah, Abrar K., Nowilaty, Sawsan R., Alhashem, Amal, Hashem, Mais, Abdulwahab, Firdous, Ibrahim, Niema, Alshidi, Tarfa, AlObeid, Eman, Alenazi, Mona M., Alzaidan, Hamad, Rahbeeni, Zuhair, Al–Owain, Mohammed, Sogaty, Sameera, Seidahmed, Mohammed Zain, Alkuraya, Fowzan S.

Volltext

Paracellin-1, a renal tight junction protein required for paracellular Mg2+ resorption von SIMON, D. B, YIN LU, MCCREDIE, D, MILFORD, D, SANJAD, S, LIFTON, R. P, CHOATE, K. A, VELAZQUEZ, H, AL-SABBAN, E, PRAGA, M, CASARI, G, BETTINELLI, A, COLUSSI, G, RODRIGUEZ-SORIANO, J

Volltext

Coexistent Linear Scleroderma and Juvenile Systemic Lupus Erythematosus von Majeed, Mahmoud, Al‐Mayouf, Sulaiman M., Al‐Sabban, Essam, Bahabri, Sultan

Volltext

Mutations in ATP6N1B, encoding a new kidney vacuolar proton pump 116-kD subunit, cause recessive distal renal tubular acidosis with preserved hearing von Smith, Annabel N., Skaug, Jennifer, Choate, Keith A., Nayir, Ahmet, Bakkaloglu, Aysin, Ozen, Seza, Hulton, Sally A., Sanjad, Sami A., Al-Sabban, Essam A., Lifton, Richard P., Scherer, Stephen W., Karet, Fiona E.

Volltext

Clinical and epidemiological assessment of steroid-resistant nephrotic syndrome associated with the NPHS2 R229Q variant von Machuca, Eduardo, Hummel, Aurélie, Nevo, Fabien, Dantal, Jacques, Martinez, Frank, Al-Sabban, Essam, Baudouin, Véronique, Abel, Laurent, Grünfeld, Jean-Pierre, Antignac, Corinne

Volltext

Paracellin-1, a Renal Tight Junction Protein Required for Paracellular Mg$^{2+}$ Resorption von Simon, David B., Lu, Yin, Choate, Keith A., Velazquez, Heino, Al-Sabban, Essam, Praga, Manuel, Casari, Giorgio, Bettinelli, Alberto, Colussi, Giacomo, Rodriguez-Soriano, Juan, McCredie, David, Milford, David, Sanjad, Sami, Lifton, Richard P.

Volltext

Hyperglycemia and Hypoinsulinemia in Patients with Fanconi-Bickel Syndrome von Taha, Doris, Al-Harbi, Naffaa, Al-Sabban, Essam

Volltext

Post renal transplantation tubulopathies in children: a 9-year experience at a tertiary care centre von Al-Ibrahim, Alia, Sanjed, Sami, Al-Abbad, Abbas, Al-Sabban, Essam, Al-Shaibani, Khalid

Volltext

The Pitfall of White Blood Cell Cystine Measurement to Diagnose Juvenile Cystinosis von Bondue, Tjessa, Kouraich, Anas, Berlingerio, Sante Princiero, Veys, Koenraad, Marie, Sandrine, Alsaad, Khaled O, Al-Sabban, Essam, Levtchenko, Elena, van den Heuvel, Lambertus

Volltext

The Pitfall of White Blood Cell Cystine Measurement to Diagnose Juvenile Cystinosis von Bondue, Tjessa, Kouraich, Anas, Berlingerio, Sante Princiero, Veys, Koenraad, Marie, Sandrine, Alsaad, Khaled O, Al-Sabban, Essam, Levtchenko, Elena, van den Heuvel, Lambertus

Volltext

Localization of a Gene for Autosomal Recessive Distal Renal Tubular Acidosis with Normal Hearing ( rdRTA2 ) to 7q33-34 von Karet, Fiona E., Finberg, Karin E., Nayir, Ahmet, Bakkaloglu, Aysin, Ozen, Seza, Hulton, Sally A., Sanjad, Sami A., Al-Sabban, Essam A., Medina, Juan F., Lifton, Richard P.

Volltext

Continuous kidney replacement therapy outcomes in infants and newborns von Sebeih, Yousef, Al-Turki, Abdullah, Alfattani, Areej, Al-Shareef, Turki, Saadeh, Sermin, Al-Sabban, Essam, Aldhaferi, Rezqah, AlHusseini, Noara, Alanzi, Fawaz, AlMaiman, Weiam

Volltext

The morbid genome of ciliopathies: an update von Shamseldin, Hanan E., Shaheen, Ranad, Ewida, Nour, Bubshait, Dalal K., Alkuraya, Hisham, Almardawi, Elham, Howaidi, Ali, Sabr, Yasser, Abdalla, Ebtesam M., Alfaifi, Abdullah Y., Mohammed Alghamdi, Jameel, Alsagheir, Afaf, Alfares, Ahmed, Morsy, Heba, Hussein, Maged H., Al-Muhaizea, Mohammad A., Shagrani, Mohammad, Al Sabban, Essam, Salih, Mustafa A., Meriki, Neama, Khan, Rubina, Almugbel, Maisoon, Qari, Alya, Tulba, Maha, Mahnashi, Mohammed, Alhazmi, Khalid, Alsalamah, Abrar K., Nowilaty, Sawsan R., Alhashem, Amal, Hashem, Mais, Abdulwahab, Firdous, Ibrahim, Niema, Alshidi, Tarfa, AlObeid, Eman, Alenazi, Mona M., Alzaidan, Hamad, Rahbeeni, Zuhair, Al-Owain, Mohammed, Sogaty, Sameera, Zain Seidahmed, Mohammed, Alkuraya, Fowzan S.

Volltext

Primary Hyperoxaluria Type I: An Underestimated Cause of Nephrocalcinosis and Chronic Renal Failure in Saudi Arabian Children von Sanjad, Sami A., Al-Abbad, Abbas, Al-Sabban, Essam

Volltext

Alport-like glomerular changes in a patient with nephrotic syndrome : report of a case von AKHTAR, M, AL-SABBAN, E

Volltext

A mutation in GLUT2, not in phosphorylase kinase subunits, in hepato-renal glycogenosis with Fanconi syndrome and low phosphorylase kinase activity von BURWINKEL, B, SANJAD, S. A, AL-SABBAN, E, AL-ABBAD, A, KILIMANN, M. W

Volltext

Paracellin-1, a Renal Tight Junction Protein Required for Paracellular [Mg.sup.2+] Resorption von Simon, David B, Lu, Yin, Choate, Keith A, Velazquez, Heino, Al-Sabban, Essam, Praga, Manuel, Casari, Giorgio, Bettinelli, Alberto, Colussi, Giacomo, Rodriguez-Soriano, Juan, McCredie, David, Milford, David, Sanjad, Sami, Lifton, Richard P

Volltext