Zobrazeno 1 - 10
of 36
pro vyhledávání: '"Valérie Anne Mclin"'
Autor:
Valérie Anne McLin, Stéphanie Franchi-Abella, Timothée Brütsch, Atessa Bahadori, Valeria Casotti, Jean de Ville de Goyet, Grégoire Dumery, Emmanuel Gonzales, Florent Guérin, Sebastien Hascoet, Nigel Heaton, Béatrice Kuhlmann, Frédéric Lador, Virginie Lambert, Paolo Marra, Aurélie Plessier, Alberto Quaglia, Anne-Laure Rougemont, Laurent Savale, Moinak Sen Sarma, Olivier Sitbon, Riccardo Antonio Superina, Hajime Uchida, Mirjam van Albada, Hubert Petrus Johannes van der Doef, Valérie Vilgrain, Julie Wacker, Nitash Zwaveling, Dominique Debray, Barbara Elisabeth Wildhaber
Publikováno v:
JHEP Reports, Vol 6, Iss 1, Pp 100933- (2024)
Summary: Congenital portosystemic shunts are often associated with systemic complications, the most challenging of which are liver nodules, pulmonary hypertension, endocrine abnormalities, and neurocognitive dysfunction. In the present paper, we offe
Externí odkaz:
https://doaj.org/article/78b59ccf97fc4fb1b0c1890877aad9c0
Autor:
Atessa Bahadori, Beatrice Kuhlmann, Dominique Debray, Stephanie Franchi-Abella, Julie Wacker, Maurice Beghetti, Barbara E. Wildhaber, Valérie Anne McLin, on behalf of the IRCPSS
Publikováno v:
Children, Vol 9, Iss 2, p 243 (2022)
Background: Congenital portosystemic shunts (CPSS) are rare vascular anomalies resulting in communications between the portal venous system and the systemic venous circulation, affecting an estimated 30,000 to 50,000 live births. CPSS can present at
Externí odkaz:
https://doaj.org/article/39a02a3780ff40c290b8a9812bb05691
Autor:
Mounif El-Youssef, Taofic Mounajjed, Ryan J. Schulze, Luz Sanchez, Rondell P. Graham, Erin Conboy, Brendan C. Lanpher, Linda Hasadsri, Jian-She Wang, Jia-Qi Li, Tanya L. Schwab, Sarah S. Barnett, Reka Kovacs-Nagy, Eric W. Klee, Monique Williams, Christian Staufner, Karl J. Clark, Robert Kopajtich, Holger Prokisch, Nathan C. Hull, Daisy Rymen, Valérie Anne Mclin, Mark A. McNiven, Roshini S. Abraham, Margot A. Cousin, Dominic Lenz, Georg F. Hoffmann, Daniela Marx-Berger, Ye Yang
Publikováno v:
Am. J. Hum. Genet. 105, 108-121 (2019)
American Journal of Human Genetics, Vol. 105, No 1 (2019) pp. 108-121
American Journal of Human Genetics, Vol. 105, No 1 (2019) pp. 108-121
Pediatric acute liver failure (ALF) is life threatening with genetic, immunologic, and environmental etiologies. Approximately half of all cases remain unexplained. Recurrent ALF (RALF) in infants describes repeated episodes of severe liver injury wi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::de9781f5b485dd30e3a06bca03bb90e0
https://push-zb.helmholtz-muenchen.de/frontdoor.php?source_opus=56338
https://push-zb.helmholtz-muenchen.de/frontdoor.php?source_opus=56338
Autor:
Alexandra Tsouka, Valérie Anne Mclin
Publikováno v:
Clinics and Research in Hepatology and Gastroenterology. 36:262-267
Children with chronic liver disease (CLD) need a head to toe approach and an early suspicion of multi organ involvement. Nutritional assessment and management is the cornerstone of management. Consider immune dysfunction in everyday treatment decisio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fc703845e9aea54e97da669e92e4d59b
https://doi.org/10.1016/j.clinre.2012.03.015
https://doi.org/10.1016/j.clinre.2012.03.015
Autor:
K. Anastaze Stelle, Valérie Anne Mclin, Eric Girardin, Dominique Charles Belli, Barbara E. Wildhaber, A. Giroud, Paloma Maria Parvex
Publikováno v:
Pediatric Transplantation. 16:250-256
The aim of this study was to analyze the impact of TAC on medium term (three-yr follow-up) renal function in pediatric liver transplant (OLT) recipients. Glomerular and tubular indices were retrospectively analyzed in 24 consecutive OLT pediatric rec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8e0989bbabf78f3a53be8ba6d00fea75
https://doi.org/10.1111/j.1399-3046.2011.01625.x
https://doi.org/10.1111/j.1399-3046.2011.01625.x
Publikováno v:
Journal of Pediatric Gastroenterology and Nutrition, Vol. 53, No 4 (2011) pp. 459-62
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3a1d5f0c45e25d42498fe493bea3871b
https://doi.org/10.1097/mpg.0b013e318216f2c7
https://doi.org/10.1097/mpg.0b013e318216f2c7
Publikováno v:
Pediatric Transplantation. 16:E172-E176
Internal hernias are an extremely rare complication after pediatric liver transplantation, and its presentation with cholestasis has not been described to date. We report the case of a 12-yr-old boy who presented with moderate abdominal pain 11 yr af
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::37d97445ad28249ef2d9f82a9573cffe
https://doi.org/10.1111/j.1399-3046.2011.01496.x
https://doi.org/10.1111/j.1399-3046.2011.01496.x
Autor:
Caroline Hastings, Judith F. Margolin, Debra L. Kearney, Valérie Anne Mclin, Jennifer R. Rushton, Amy Kun Pass
Publikováno v:
Journal of Pediatric Hematology / Oncology, Vol. 30, No 12 (2008) pp. 976-980
This is the first description in which the diagnosis of vanishing bile duct syndrome (VBDS) preceded the diagnosis of Hodgkin disease (HD) by several months, and for which patients received modifications to modern MOPP-ABV chemotherapy with successfu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::315e6ccfb72e4e1a5b5f91b35aa34635
https://doi.org/10.1097/mph.0b013e31818b37c4
https://doi.org/10.1097/mph.0b013e31818b37c4