Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Madeleine Thibault"'
Autor:
Ashley M. Toye, Jean Delaunay, Brigitte Bader-Meunier, Moudji Khanfar, Gil Tchernia, Madeleine Thibault, Thérèse Cynober, Lesley J. Bruce, Rosalind C. Williamson, Michèle Dechaux
Publikováno v:
Blood
We describe a mutation in human erythrocyte band 3 (anion exchanger 1; SLC4A1) causing both hereditary spherocytosis and distal renal tubular acidosis. The proband developed a transfusion-dependent, hemolytic anemia following birth. Immunoblotting sh
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6ba28f26630c15a8d7d5e13e63d892a8
https://doi.org/10.1182/blood-2007-07-099473
https://doi.org/10.1182/blood-2007-07-099473
Autor:
Narla Mohandas, Gil Tchernia, Véronique Picard, Thomas Pincez, Guénolée de Lambert, Loïc Garçon, Madeleine Thibault, Frédéric Gauthier, Corinne Guitton
Publikováno v:
Blood. 126:276-276
Total splenectomy is recommended in symptomatic cases of hereditary spherocytosis (HS) to reduce the severity of anemia but exposes patients to long-term infectious or thrombotic complications. Alternative strategies such as subtotal splenectomy (STS
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::68f0f4d688791bd7bad02bbecccc845d
https://doi.org/10.1182/blood.v126.23.276.276
https://doi.org/10.1182/blood.v126.23.276.276
Publikováno v:
Critical care medicine. 18(1)
Vitamin E (Vit E) is an important component of the lung's defense against oxidant injury. The aim of this study was to determine a) if adult respiratory distress syndrome (ARDS) was associated with a decrease in Vit E plasma level linked to an enhanc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::61b6782bb78908b673e819ace913b155
https://pubmed.ncbi.nlm.nih.gov/2293967
https://pubmed.ncbi.nlm.nih.gov/2293967
Autor:
Moudji Khanfar, Brigitte Bader-Meunier, Ashley M. Toye, Madeleine Thibault, G. Tchernia, Lesley J. Bruce, Jean Delaunay, Michèle Dechaux, Thérèse Cynober, Rosalind C. Williamson
Publikováno v:
Blood. 108:1563-1563
We describe the second case of a homozygous mutation in band 3 (anion exchanger 1 (AE1), SLC4A1) causing both hereditary spherocytosis (HS) and distal renal tubular acidosis (dRTA). This new variant differed from the previous homozygous variant (Band
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e4880077d46da7bb71c443c955de206c
https://doi.org/10.1182/blood.v108.11.1563.1563
https://doi.org/10.1182/blood.v108.11.1563.1563