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The Journal of Pediatrics|February 1, 1996
Natural history of Alström syndrome in early childhood: onset with dilated cardiomyopathyJ L Michaud, E Héon, F Guilbert, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|December 1, 2010
[Dietetic treatment of cow's milk protein allergy]C Dupont, J-P Chouraqui, D de Boissieu, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|September 15, 2022
"Baby-led weaning" - Progress in infant feeding or risky trend?A Bocquet, S Brancato, D Turck, et al.
Human Molecular Genetics|May 1, 2014
The genetic landscape of infantile spasmsJacques L Michaud, Mathieu Lachance, Fadi F Hamdan, et al.
Gastroenterologie Clinique Et Biologique|March 23, 2010
Treatments for pediatric achalasia: Heller myotomy or pneumatic dilatation?C Jung, L Michaud, J-F Mougenot, et al.
Neurology. Genetics|November 11, 2016
FHF1 (FGF12) epileptic encephalopathySameer Al-Mehmadi, Miranda Splitt, , et al.
European Journal of Human Genetics : EJHG|November 21, 2013
Single exon-resolution targeted chromosomal microarray analysis of known and candidate intellectual disability genesTracy Tucker, Farah R Zahir, Malachi Griffith, et al.
Molecular Genetics & Genomic Medicine|November 12, 2018
Whole exome sequencing identifies novel predisposing genes in neural tube defectsPhilippe Lemay, Patrizia De Marco, Monica Traverso, et al.
Population Health Management|March 28, 2018
Remote Patient Monitoring and Clinical Outcomes for Postdischarge Patients with Type 2 DiabetesTzeyu L Michaud, Mohammad Siahpush, Robert J Schwab, et al.
Human Mutation|October 4, 2012
Identification of novel mutations confirms PDE4D as a major gene causing acrodysostosisDanielle C Lynch, David A Dyment, Lijia Huang, et al.
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