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.

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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

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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.

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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.

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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

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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.

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

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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

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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.

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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

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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.

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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

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

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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.

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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

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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

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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

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

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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

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COXIELLA BURNETII ENDOCARDITIS IN A CHILD von Al-Hajjar, Sami, Hussain Qadri, S M, Al-Sabban, Essam, Jäger, Cornelie

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