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M.E. Bouma

Observed names: Bouma, M.E., M E Bouma, M Samson-Bouma, M. -E. Bouma, M. E. Bouma, M. E. Samson-Bouma, M.-E. Bouma, M.-E. Samson-Bouma, M.E. Bouma-Samson, M.E. Samson-Bouma, M.‐E. BOUMA, ME Bouma, ME Samson‐Bouma, Marie E Samson-Bouma, Marie Elisabeth Samson-Bouma, Marie-Elisabeth BOUMA, Marie-Elisabeth Bouma, Marie-Elisabeth Samson-Bouma, Marie-Elizabeth Samson-Bouma, Marie-elisabeth Samson-bouma, Marie‐Elisabeth Samson‐Bouma
Observed institutions: Hôpital Necker-Enfants Malades, Centre National de la Recherche Scientifique, Inserm, Université Paris Cité, Sorbonne Paris Cité, Bristol-Myers Squibb (United States), Hôpital Saint-Antoine, Laboratoire de Biochimie, Health and Functional Exposomics, Hôpital Avicenne, Laboratoire de Recherche Vasculaire Translationnelle, Centre de Recherche Saint-Antoine, Institut du Thorax, Hôpital Bichat-Claude-Bernard, Centre de Génétique Moléculaire, Université Paris Diderot, Université Paris Descartes
OpenAlex ID: A5112166770
Absence of Microsomal Triglyceride Transfer Protein in Individuals with Abetalipoproteinemia
1992 · John R. Wetterau, Lawrence P. Aggerbeck, et al. · Science · 763
The Role of the Microsomal Triglygeride Transfer Protein in Abetalipoproteinemia
2000 · N. Berriot-Varoqueaux, L. P. Aggerbeck, et al. · Annual Review of Nutrition · 312
Molecular analysis and intestinal expression of SAR1 genes and proteins in Anderson's disease (Chylomicron retention disease)
2011 · Amandine Georges, Jessica Bonneau, et al. · Orphanet Journal of Rare Diseases · 178
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Homozygous MTTP and APOB mutations may lead to hepatic steatosis and fibrosis despite metabolic differences in congenital hypocholesterolemia
2014 · Mathilde Di Filippo, Philippe Moulin, et al. · Journal of Hepatology · 153
Further cellular investigation of the human hepatoblastoma-derived cell line HepG2: Morphology and immunocytochemical studies of hepatic-secreted proteins
1989 · Marie-Elisabeth Bouma, Edith Rogier, et al. · In Vitro Cellular & Developmental Biology - Plant · 128
Isolation, Culture and Characterization of Adult Human Hepatocytes from Surgical Liver Biopsies
1984 · Francois Ballet, Marie-Elisabeth Bouma, et al. · Hepatology · 84
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A Novel Abetalipoproteinemia Genotype
1996 · Edward F. Rehberg, Marie-Elisabeth Samson-Bouma, et al. · Journal of Biological Chemistry · 82
Hypobetalipoproteinemia with accumulation of an apoprotein B-like protein in intestinal cells. Immunoenzymatic and biochemical characterization of seven cases of Anderson's disease.
1986 · M E Bouma, I Beucler, et al. · Journal of Clinical Investigation · 80
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Anderson’s Disease
1999 · A. Hayssam Dannoura, Nathalie Berriot-Varoqueaux, et al. · Arteriosclerosis Thrombosis and Vascular Biology · 66
Apolipoprotein B48 glycosylation in abetalipoproteinemia and Anderson's disease
2001 · Nathalie Berriot-Varoqueaux, A.Hayssam Dannoura, et al. · Gastroenterology · 57
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Molecular and functional analysis of two new MTTP gene mutations in an atypical case of abetalipoproteinemia
2012 · Mathilde Di Filippo, Hervé Créhalet, et al. · Journal of Lipid Research · 51
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Chylomicron retention disease: A long term study of two cohorts
2009 · Noel Peretti, Claude C. Roy, et al. · Molecular Genetics and Metabolism · 48
Anderson’s disease (chylomicron retention disease): a new mutation in the SARA2 gene associated with muscular and cardiac abnormalities
2008 · M Silvain, D Bligny, et al. · Clinical Genetics · 43
Microvillous Atrophy
2014 · Ariane Perry, Hayet Bensallah, et al. · Journal of Pediatric Gastroenterology and Nutrition · 41
Description of two different patients with abetalipoproteinemia: synthesis of a normal-sized apolipoprotein B-48 in intestinal organ culture.
1990 · ME Bouma, I Beucler, et al. · Journal of Lipid Research · 39
Strategies for proprotein convertase subtilisin kexin 9 modulation: a perspective on recent patents
2010 · Marianne Abifadel, Jihane Pakradouni, et al. · Expert Opinion on Therapeutic Patents · 33
Decreased expression of Intestinal I- and L-FABP levels in rare human genetic lipid malabsorption syndromes
2007 · S. Guilmeau, I. Niot, et al. · Histochemistry and Cell Biology · 30
Anderson's disease/chylomicron retention disease in a Japanese patient with uniparental disomy 7 and a normal SAR1B gene protein coding sequence
2011 · Tomoo Okada, Michio Miyashita, et al. · Orphanet Journal of Rare Diseases · 27
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High-Yield Preparation of Porcine Hepatocytes for Long Survival after Transplantation in the Spleen
2008 · B. Nordlinger, M.E. Bouma, et al. · European Surgical Research · 27
Chylomicron retention disease
1988 · M.E. Bouma, R. Infante, et al. · Gastroenterology · 26
Plasma lipoproteins in infantile visceral Leishmaniasis: deficiency of apolipoproteins A-I and A-II
1989 · Etienne D. Bekaert, Rekaya Kallel, et al. · Clinica Chimica Acta · 25
Alterations in lipoprotein density classes in infantile visceral Leishmaniasis: presence of apolipoprotein SAA
1992 · E. D. BEKAERT, E. DOLE, et al. · European Journal of Clinical Investigation · 24
Synthesis and secretion of lipoproteins by human hepatocytes in culture
1988 · M. E. Bouma, M. Pessah, et al. · In Vitro Cellular & Developmental Biology - Plant · 21
Can Hepatocytes Proliferate when Transplanted into the Spleen?
2008 · B. Nordlinger, S.R. Wang, et al. · European Surgical Research · 20
Apolipoprotein B Production and Very Low Density Lipoprotein Secretion by Calf Liver Slices
1999 · D. Gruffat-Mouty, B. Graulet, et al. · The Journal of Biochemistry · 19
Works count: 64
Citation count: 2,560
H-index: 22
I10-index: 36
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