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Brigitte Pothier

Sp alpha V/41: a common spectrin polymorphism at the alpha IV-alpha V domain junction. Relevance to the expression level of hereditary elliptocytosis due to alpha-spectrin variants located in trans.
1991 · N Alloisio, L Morlé, et al. · Journal of Clinical Investigation · 65
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Two elliptocytogenic alpha I/74 variants of the spectrin alpha I domain. Spectrin Culoz (GGT----GTT; alpha I 40 Gly----Val) and spectrin Lyon (CTT----TTT; alpha I 43 Leu---Phe).
1990 · L Morlé, A F Roux, et al. · Journal of Clinical Investigation · 39
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The red cell skeleton and its genetic disorders
1990 · Jean Delaunay, Nicole Alloisio, et al. · Molecular Aspects of Medicine · 39
A haemolytic syndrome associated with the complete absence of red cell membrane protein 4.2 in two Tunisian siblings
1990 · A. Ghanem, B. Pothier, et al. · British Journal of Haematology · 36
Spα1/65 hereditary elliptocytosis in North Africa
1986 · N. Alloisio, D. Guetarni, et al. · American Journal of Hematology · 36
Spectrin Nice (beta 220/216): a shortened beta-chain variant associated with an increase of the alpha I/74 fragment in a case of elliptocytosis
1987 · B Pothier, L Morle, et al. · Blood · 34
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Reduction of membrane band 7 and activation of volume stimulated (K+, Cl−)‐cotransport in a case of congenital stomatocytosis
1989 · L. Morlé, B. Pothier, et al. · British Journal of Haematology · 33
An insertional frameshift mutation of the beta-spectrin gene associated with elliptocytosis in spectrin nice (beta 220/216)
1991 · WT Tse, PG Gallagher, et al. · Blood · 26
Spectrin Oran (alpha II/21), a new spectrin variant concerning the alpha II domain and causing severe elliptocytosis in the homozygous state
1988 · N Alloisio, L Morle, et al. · Blood · 26
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Occurrence of the αI 22 Arg→His (CGT→CAT) spectrin mutation in Tunisia: potential association with severe elliptopoikilocytosis
1991 · F. Baklouti, J. Marechal, et al. · British Journal of Haematology · 20
Assignment of Sp alpha I/74 hereditary elliptocytosis to the alpha- or beta-chain of spectrin through in vitro dimer reconstitution
1990 · B Pothier, N Alloisio, et al. · Blood · 16
Spectrin Tunis (alpha I/78): a new alpha I variant that causes asymptomatic hereditary elliptocytosis in the heterozygous state
1988 · L Morle, N Alloisio, et al. · Blood · 12
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Aberrant pattern of red cell membrane and cytosolic proteins in a case of congenital dyserythropoietic anaemia
1987 · Brigitte Pothier, Laurette Morlea, et al. · British Journal of Haematology · 8
Two distinct variants of erythrocyte spectrin ?IV domain
1989 · B. Pothier, N. Alloisio, et al. · Human Genetics · 4
Red cell membrane alteration involving protein 4.1 and protein 3 in a case of recessively inherited haemolytic anaemia
1987 · Laurette Morlé, Brigitte Pothier, et al. · European Journal Of Haematology · 2
[Interaction between various alkylxanthines and the proteins of the erythrocyte skeleton].
1988 · J Delaunay, B Pothier, et al. · PubMed
Études structurales et fonctionnelles des protéines du squelette membranaire du globule rouge humain : découverte d'anomalies nouvelles au cours de syndromes hémolytiques constitutionnels
1987 · B Pothier
Works count: 17
Citation count: 396
H-index: 12
I10-index: 12
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