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I Maire

Showing results (31-40 of 121) with videos related to

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European Journal of Human Genetics : EJHG|January 1, 1996
Types I and III Gaucher disease in Poland: incidence of the most common mutations and phenotypic manifestationsA Tylki-Szymańska, G Millat, I Maire, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|April 30, 1996
Amniotic fluid for screening of lysosomal storage diseases presenting in utero (mainly as non-immune hydrops fetalis)M Piraud, R Froissart, G Mandon, et al.
Journal of Neurology|February 14, 1978
Erythrocyte ghost (Na+ + K+) ATPase activity in mice with hereditary muscular dystrophy (strain C57 BL/64J/dy)G Souweine, M O Rolland, I Maire, et al.
Journal of Medical Genetics|February 1, 1997
Germline and somatic mosaicism in a female carrier of Hunter diseaseR Froissart, I Maire, V Bonnet, et al.
The Biochemical Journal|July 15, 1995
Processing of iduronate 2-sulphatase in human fibroblastsR Froissart, G Millat, M Mathieu, et al.
The Journal of Pediatrics|July 22, 1998
Follow-up of nine patients with Hurler syndrome after bone marrow transplantationN Guffon, G Souillet, I Maire, et al.
Biochimica Et Biophysica Acta|September 29, 1999
The 2.1-, 5.4- and 5.7-kb transcripts of the IDS gene are generated by different polyadenylation signalsS Cudry, R Froissart, O Bouton, et al.
Clinical Biochemistry|April 1, 1991
Biochemical diagnosis of hepatic glycogen storage diseases: 20 years French experienceI Maire, C Baussan, N Moatti, et al.
European Journal of Pediatrics|February 1, 1988
Prevention of neonatal hypoglycaemia by oral lipid supplementation in low birth weight infantsL Sann, B Mousson, M Rousson, et al.
Journal of Physiology and Pharmacology : an Official Journal of the Polish Physiological Society|December 1, 1993
Acid and neutral lipase activity in lymphocytes of patients with increased serum cholesterol and triglyceride levelB Miszczuk-Jamska, F Chevalier, I Maire, et al.
Pageof 13

Showing results (31-40 of 121) with videos related to

Sort By:
Pageof 13
European Journal of Human Genetics : EJHG|January 1, 1996
Types I and III Gaucher disease in Poland: incidence of the most common mutations and phenotypic manifestationsA Tylki-Szymańska, G Millat, I Maire, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|April 30, 1996
Amniotic fluid for screening of lysosomal storage diseases presenting in utero (mainly as non-immune hydrops fetalis)M Piraud, R Froissart, G Mandon, et al.
Journal of Neurology|February 14, 1978
Erythrocyte ghost (Na+ + K+) ATPase activity in mice with hereditary muscular dystrophy (strain C57 BL/64J/dy)G Souweine, M O Rolland, I Maire, et al.
Journal of Medical Genetics|February 1, 1997
Germline and somatic mosaicism in a female carrier of Hunter diseaseR Froissart, I Maire, V Bonnet, et al.
The Biochemical Journal|July 15, 1995
Processing of iduronate 2-sulphatase in human fibroblastsR Froissart, G Millat, M Mathieu, et al.
The Journal of Pediatrics|July 22, 1998
Follow-up of nine patients with Hurler syndrome after bone marrow transplantationN Guffon, G Souillet, I Maire, et al.
Biochimica Et Biophysica Acta|September 29, 1999
The 2.1-, 5.4- and 5.7-kb transcripts of the IDS gene are generated by different polyadenylation signalsS Cudry, R Froissart, O Bouton, et al.
Clinical Biochemistry|April 1, 1991
Biochemical diagnosis of hepatic glycogen storage diseases: 20 years French experienceI Maire, C Baussan, N Moatti, et al.
European Journal of Pediatrics|February 1, 1988
Prevention of neonatal hypoglycaemia by oral lipid supplementation in low birth weight infantsL Sann, B Mousson, M Rousson, et al.
Journal of Physiology and Pharmacology : an Official Journal of the Polish Physiological Society|December 1, 1993
Acid and neutral lipase activity in lymphocytes of patients with increased serum cholesterol and triglyceride levelB Miszczuk-Jamska, F Chevalier, I Maire, et al.
Pageof 13