H. Boutignon

Infantile hypercalcemia and hypercalciuria: new insights into a vitamin D-dependent mechanism and response to ketoconazole treatment.

E. Mallet, A. Linglart, M. Garabédian, 2010, The Journal of pediatrics.

Reverse cascade screening of newborns for hereditary haemochromatosis: a model for other late onset diseases?

C. Julier, K. Robson, J. Rochette, 2005, Journal of Medical Genetics.

[Fortified milk and supplements of oral vitamin D. Comparison of the effect of two doses of vitamin D (500 and 1,000 UI/d) during the first trimester of life].

M. Garabédian, O. Walrant-Debray, C. Vervel, 1997, Archives de pediatrie : organe officiel de la Societe francaise de pediatrie.

Subclinical vitamin D deficiency in neonates: definition and response to vitamin D supplements.

M. Garabédian, O. Walrant-Debray, C. Vervel, 1997, The American journal of clinical nutrition.

Immune thrombocytopenia in a newborn from a mother with primary antiphospholipid syndrome

C. Kaplan, L. Darnige, E. Benhamou, 2004, American journal of hematology.

Hyporeninemic hypoaldosteronism in infancy: a familial disease.

P. Corvol, K. Nahoul, J. Job, 1984, The Journal of clinical endocrinology and metabolism.

[Exposure of a cohort of newborn infants to tuberculosis in a neonatology service].

C. Vervel, H. Boutignon, S. Dubrulle, 2010, Archives de pediatrie : organe officiel de la Societe francaise de pediatrie.

Ureaplasma parvum meningitis in a full-term newborn.

V. Biran, O. Baud, E. Bingen, 2010, The Pediatric infectious disease journal.

[Smith-Lemli-Opitz syndrome with male pseudohermaphroditism. A case report with endocrinological study (author's transl)].

J. Limal, J. Retbi, H. Boutignon, 1981, Annales de pediatrie.