C. De laet

Deficiency of Subunit 6 of the Conserved Oligomeric Golgi Complex (COG6-CDG): Second Patient, Different Phenotype.

G. Matthijs, D. Garozzo, H. Souayah, 2012, JIMD Reports.

Nutritional status of neurologically impaired children: Impact on comorbidity.

B. Dan, K. Pelc, E. Dain, 2019, Archives de pediatrie : organe officiel de la Societe francaise de pediatrie.

Pitfalls of ketogenic diet in a neonate.

B. Dan, C. Ferreiro, P. Goyens, 2002, Pediatrics.

Phenotypic Overlap between Infantile Systemic Lupus Erythematosus and Aicardi-Goutières Syndrome

B. Dan, F. Mascart, C. Christophe, 2005, Neuropediatrics.

Unilateral bowing of long bones and multiple congenital anomalies in a child born to a mother with gestational diabetes.

G. Mortier, E. Vamos, W. Courtens, 2000, Annales de genetique.

[Newborn screening : the point of view of the paediatrician].

A. Mansbach, B. Gulbis, A. Ferster, 2015, Revue medicale de Bruxelles.

Cutaneous porphyria in a neonate with tyrosinaemia type 1

S. Vanden Eijnden, E. Vamos, A. Clercx, 2000, European Journal of Pediatrics.

Late-treated phenylketonuria mimicking Angelman syndrome.

B. Dan, P. Goyens, C. De laet, 2001, American journal of medical genetics.