Influenza-associated thrombotic microangiopathies

por Bitzan, Martin, Zieg, Jakub
Publicado 2017

Postinfectious Hemolytic Uremic Syndrome

por Bitzan, Martin, Lapeyraque, Anne-Laure
Publicado 2016

Recurrent Focal Segmental Glomerulosclerosis: A Discrete Clinical Entity

por Torban, Elena, Bitzan, Martin, Goodyer, Paul
Publicado 2012

Rituximab in Minimal Change Disease: Mechanisms of Action and Hypotheses for Future Studies

por Madanchi, Nima, Bitzan, Martin, Takano, Tomoko
Publicado 2017

Erratum to “Endolymphatic Sac Enlargement in a Girl with a Novel Mutation for Distal Renal Tubular Acidosis and Severe Deafness”

por Rink, Nikki, Bitzan, Martin, O'Gorman, Gus, Nagel, Mato, Torban, Elena, Goodyer, Paul
Publicado 2013

Efficacy and safety of levamisole in childhood nephrotic syndrome: A meta-analysis

por Bhatt, Girish Chandra, Patel, Bhupeshwari, Das, Rashmi Ranjan, Malik, Shikha, Bitzan, Martin, Mishra, Nihar Ranjan
Publicado 2023

Acquired thrombotic thrombocytopenic purpura with isolated CFHR3/1 deletion—rapid remission following complement blockade

por Bitzan, Martin, Hammad, Rawan M., Bonnefoy, Arnaud, Al Dhaheri, Watfa Shahwan, Vézina, Catherine, Rivard, Georges-Étienne
Publicado 2018

Setting New Directions for Research in Childhood Nephrotic Syndrome: Results From a National Workshop

por Samuel, Susan M., Takano, Tomoko, Scott, Shannon, Benoit, Genevieve, Bitzan, Martin, Mammen, Cherry, Ryan, Laurel, Morgan, Catherine
Publicado 2017

Native nephrectomy prior to pediatric kidney transplantation: biological and clinical aspects

por Ghane Sharbaf, Fatemeh, Bitzan, Martin, Szymanski, Konrad M., Bell, Lorraine E., Gupta, Indra, Tchervenkov, Jean, Capolicchio, John-Paul
Publicado 2012

Relapsing and refractory peritoneal dialysis peritonitis caused by Corynebacterium amycolatum

por Habeeb, Shameer M., Yamin, Haneen, Simkova, Eva, Awad, Hazem S., Alhammadi, Entesar A., Eid, Loai A., Lone, Rubina, Bitzan, Martin
Publicado 2022

Case Report: Guillain-Barré Syndrome as Primary Presentation of Systemic Lupus Erythematosus (SLE-GBS) in a Teenage Girl

por Beshir, Elham, Belt, Ernestina, Chencheri, Nidheesh, Saqib, Aqdas, Pallavidino, Marco, Terheggen, Ulrich, Abdalla, Abdalla, Herlitz, Leal, Sharif, Elsadeg, Bitzan, Martin
Publicado 2022

Case Report: CMV-Associated Congenital Nephrotic Syndrome

por Jacob, Anju, Habeeb, Shameer M., Herlitz, Leal, Simkova, Eva, Shekhy, Jwan F., Taylor, Alan, Abuhammour, Walid, Abou Tayoun, Ahmad, Bitzan, Martin
Publicado 2020

The extrafollicular B cell response is a hallmark of childhood idiopathic nephrotic syndrome

por Al-Aubodah, Tho-Alfakar, Aoudjit, Lamine, Pascale, Giuseppe, Perinpanayagam, Maneka A., Langlais, David, Bitzan, Martin, Samuel, Susan M., Piccirillo, Ciriaco A., Takano, Tomoko
Publicado 2023

The Canadian childhood nephrotic syndrome (CHILDNEPH) study: report on mid-study feasibility, recruitment and main measures

por Samuel, Susan M., Dart, Allison, Filler, Guido, Bitzan, Martin, Pinsk, Maury, Mammen, Cherry, Nettel-Aguirre, Alberto, Perinpanayagam, Maneka A., Takano, Tomoko, Chanchlani, Rahul, Zappitelli, Michael
Publicado 2019

Intrinsic tumor necrosis factor-α pathway is activated in a subset of patients with focal segmental glomerulosclerosis

por Chung, Chen-Fang, Kitzler, Thomas, Kachurina, Nadezda, Pessina, Katarina, Babayeva, Sima, Bitzan, Martin, Kaskel, Frederic, Colmegna, Ines, Alachkar, Nada, Goodyer, Paul, Cybulsky, Andrey V., Torban, Elena
Publicado 2019

Clinical Characteristics and Outcome of Canadian Patients Diagnosed With Atypical Hemolytic Uremic Syndrome

por Lapeyraque, Anne-Laure, Bitzan, Martin, Al-Dakkak, Imad, Francis, Mira, Huang, Shih-Han S., Kaprielian, Roger, Larratt, Loree, Pavenski, Katerina, Ribic, Christine, Tosikyan, Axel, Licht, Christoph, Philibert, David
Publicado 2020

Making the Correct Diagnosis in Thrombotic Microangiopathy: A Narrative Review

por McFarlane, Philip A., Bitzan, Martin, Broome, Catherine, Baran, Dana, Garland, Jocelyn, Girard, Louis-Philippe, Grewal, Kuljit, Lapeyraque, Anne-Laure, Patriquin, Christopher Jordan, Pavenski, Katerina, Licht, Christoph
Publicado 2021

ARHGDIA: a novel gene implicated in nephrotic syndrome

por Gupta, Indra Rani, Baldwin, Cindy, Auguste, David, Ha, Kevin C H, El Andalousi, Jasmine, Fahiminiya, Somayyeh, Bitzan, Martin, Bernard, Chantal, Akbari, Mohammad Reza, Narod, Steven A, Rosenblatt, David S, Majewski, Jacek, Takano, Tomoko
Publicado 2013

The Canadian Childhood Nephrotic Syndrome (CHILDNEPH) Project: overview of design and methods

por Samuel, Susan, Scott, Shannon, Morgan, Catherine, Dart, Allison, Mammen, Cherry, Parekh, Rulan, Nettel-Aguirre, Alberto, Eddy, Allison, Flynn, Rachel, Pinsk, Maury, Wade, Andrew, Arora, Steven, Benoit, Geneviève, Bitzan, Martin, Erickson, Robin, Feber, Janusz, Filler, Guido, Geier, Pavel, Girardin, Colette, Grisaru, Silviu, Tee, James, Kemp, Kyle, Zappitelli, Michael
Publicado 2014

Rapid whole genome sequencing of critically ill pediatric patients from genetically underrepresented populations

por Halabi, Nour, Ramaswamy, Sathishkumar, El Naofal, Maha, Taylor, Alan, Yaslam, Sawsan, Jain, Ruchi, Alfalasi, Roudha, Shenbagam, Shruti, Bitzan, Martin, Yavuz, Lemis, Abulhoul, Hamda, Shankar, Shiva, Janjua, Dalwinder, Jadhav, Devendrasing, Al Maazmi, Munira Mahmoud, Abuhammour, Walid, Alsheikh-Ali, Alawi, Al Awadhi, Mohamed, Al Khayat, Abdulla, Abou Tayoun, Ahmad N.
Publicado 2022