Zobrazeno 1 - 10
of 109
pro vyhledávání: '"Martin Bitzan"'
Autor:
Tho-Alfakar Al-Aubodah, Lamine Aoudjit, Giuseppe Pascale, Maneka A. Perinpanayagam, David Langlais, Martin Bitzan, Susan M. Samuel, Ciriaco A. Piccirillo, Tomoko Takano
Publikováno v:
Nature Communications, Vol 14, Iss 1, Pp 1-15 (2023)
Abstract The efficacy of the B cell-targeting drug rituximab (RTX) in childhood idiopathic nephrotic syndrome (INS) suggests that B cells may be implicated in disease pathogenesis. However, B cell characterization in children with INS remains limited
Externí odkaz:
https://doaj.org/article/3198131b69e949b9b55e707e738b0f51
Autor:
Maha El Naofal, Sathishkumar Ramaswamy, Ali Alsarhan, Ahmed Nugud, Fatima Sarfraz, Hiba Janbaz, Alan Taylor, Ruchi Jain, Nour Halabi, Sawsan Yaslam, Roudha Alfalasi, Shruti Shenbagam, Fatma Rabea, Martin Bitzan, Lemis Yavuz, Deena Wafadari, Hamda Abulhoul, Shiva Shankar, Munira Al Maazmi, Ruba Rizk, Zeinab Alloub, Haitham Elbashir, Mohamed O. E. Babiker, Nidheesh Chencheri, Ammar AlBanna, Meshal Sultan, Mohamed El Bitar, Safeena Kherani, Nandu Thalange, Sattar Alshryda, Roberto Di Donato, Christos Tzivinikos, Ibrar Majid, Alexandra F. Freeman, Corina Gonzalez, Arif O. Khan, Hisham Hamdan, Walid Abuhammour, Mohamed AlAwadhi, Abdulla AlKhayat, Alawi Alsheikh-Ali, Ahmad N. Abou Tayoun
Publikováno v:
Genome Medicine, Vol 15, Iss 1, Pp 1-12 (2023)
Abstract Background Rare diseases collectively impose a significant burden on healthcare systems, especially in underserved regions, like the Middle East, which lack access to genomic diagnostic services and the associated personalized management pla
Externí odkaz:
https://doaj.org/article/35ba5f303bf24df8a72a134940d5e4d5
Autor:
Nour Halabi, Sathishkumar Ramaswamy, Maha El Naofal, Alan Taylor, Sawsan Yaslam, Ruchi Jain, Roudha Alfalasi, Shruti Shenbagam, Martin Bitzan, Lemis Yavuz, Hamda Abulhoul, Shiva Shankar, Dalwinder Janjua, Devendrasing Jadhav, Munira Mahmoud Al Maazmi, Walid Abuhammour, Alawi Alsheikh-Ali, Mohamed Al Awadhi, Abdulla Al Khayat, Ahmad N. Abou Tayoun
Publikováno v:
Genome Medicine, Vol 14, Iss 1, Pp 1-5 (2022)
Abstract We describe a case series of five infants (age range: 1–90 days; 4 females and 1 male) who presented to Al Jalila Children’s intensive care units (ICU) with complex multisystem disorders. Patients were Emirati, Kenyan, Jordanian, Filipin
Externí odkaz:
https://doaj.org/article/21b7a0073f4d43f3a71aec8a07f493f5
Autor:
Elham Beshir, Ernestina Belt, Nidheesh Chencheri, Aqdas Saqib, Marco Pallavidino, Ulrich Terheggen, Abdalla Abdalla, Leal Herlitz, Elsadeg Sharif, Martin Bitzan
Publikováno v:
Frontiers in Pediatrics, Vol 10 (2022)
Peripheral nervous system involvement accounts for fewer than 10% of SLE cases with neuropsychiatric manifestations. Guillain-Barré syndrome (GBS) as the presenting, major manifestation of pediatric SLE is extremely rare, and the best treatment appr
Externí odkaz:
https://doaj.org/article/df6e9ba544514482bb51f09fe47c6ec0
Autor:
Philip A. McFarlane, Martin Bitzan, Catherine Broome, Dana Baran, Jocelyn Garland, Louis-Philippe Girard, Kuljit Grewal, Anne-Laure Lapeyraque, Christopher Jordan Patriquin, Katerina Pavenski, Christoph Licht
Publikováno v:
Canadian Journal of Kidney Health and Disease, Vol 8 (2021)
Purpose of review: Thrombotic microangiopathy (TMA) is suspected in patients presenting with thrombocytopenia and evidence of a microangiopathic hemolytic anemia. Patients with TMA can be critically ill, so rapid and accurate identification of the un
Externí odkaz:
https://doaj.org/article/ec3e20004dbc4da7ae2ac0595c5deed5
Autor:
Susan M. Samuel, Allison Dart, Guido Filler, Martin Bitzan, Maury Pinsk, Cherry Mammen, Alberto Nettel-Aguirre, Maneka A. Perinpanayagam, Tomoko Takano, Rahul Chanchlani, Michael Zappitelli, other members of the Canadian Childhood Nephrotic Syndrome Project Team
Publikováno v:
BMC Nephrology, Vol 20, Iss 1, Pp 1-10 (2019)
Abstract Background To assess reasons for continuing practice variation in the management of childhood nephrotic syndrome despite expert reviews and guidelines, we are conducting a longitudinal cohort study in children with glucocorticoid sensitive n
Externí odkaz:
https://doaj.org/article/93ac3ca66bae42fb8e62b155e3c8cf35
Autor:
Anju Jacob, Shameer M. Habeeb, Leal Herlitz, Eva Simkova, Jwan F. Shekhy, Alan Taylor, Walid Abuhammour, Ahmad Abou Tayoun, Martin Bitzan
Publikováno v:
Frontiers in Pediatrics, Vol 8 (2020)
Background: Congenital nephrotic syndrome, historically defined by the onset of large proteinuria during the first 3 months of life, is a rare clinical disorder, generally with poor outcome. It is caused by pathogenic variants in genes associated wit
Externí odkaz:
https://doaj.org/article/b0a1794ad07a4ca8b5608927b2cac373
Autor:
Anne-Laure Lapeyraque, Martin Bitzan, Imad Al-Dakkak, Mira Francis, Shih-Han S. Huang, Roger Kaprielian, Loree Larratt, Katerina Pavenski, Christine Ribic, Axel Tosikyan, Christoph Licht, David Philibert
Publikováno v:
Canadian Journal of Kidney Health and Disease, Vol 7 (2020)
Background: Atypical hemolytic uremic syndrome (aHUS) is an extremely rare, heterogeneous disease of uncontrolled activation of the alternative complement pathway that is difficult to diagnose. We have evaluated the Canadian patients enrolled in the
Externí odkaz:
https://doaj.org/article/f5abb0f45f7045dab2ce21463229fe09
Autor:
Chen-Fang Chung, Thomas Kitzler, Nadezda Kachurina, Katarina Pessina, Sima Babayeva, Martin Bitzan, Frederic Kaskel, Ines Colmegna, Nada Alachkar, Paul Goodyer, Andrey V Cybulsky, Elena Torban
Publikováno v:
PLoS ONE, Vol 14, Iss 5, p e0216426 (2019)
Focal segmental glomerulosclerosis (FSGS) is frequently found in biopsies of patients with steroid resistant nephrotic syndrome (SRNS). The pathogenesis of SRNS/FSGS is often unknown and the disease will recur in up to 50% of patients post-transplant
Externí odkaz:
https://doaj.org/article/c04c71e4770b4b228a62cc2680a5e847
Autor:
Susan M. Samuel, Tomoko Takano, Shannon Scott, Genevieve Benoit, Martin Bitzan, Cherry Mammen, Laurel Ryan, Catherine Morgan
Publikováno v:
Canadian Journal of Kidney Health and Disease, Vol 4 (2017)
Background: We report on the proceedings of a national workshop held in Canada with the aims to identify priorities for research in childhood nephrotic syndrome and to develop a national strategy to address these priorities. Methods: A diverse group
Externí odkaz:
https://doaj.org/article/fd2eb010a2bb401fabc74e8a999889e0