P. Goyens

发表

Key features and clinical variability of COG6-CDG.

Gert Matthijs, Uwe Kornak, Hubertus C M T Prinsen, 2015, Molecular genetics and metabolism.

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.

Effects of thirty elements on bone metabolism.

G. Lognay, P. Goyens, M. Dermience, 2015, Journal of trace elements in medicine and biology : organ of the Society for Minerals and Trace Elements.

Malnutrition and Diarrhea: Working Group Report of the First World Congress of Pediatric Gastroenterology, Hepatology, and Nutrition

Z. Bhutta, J. Udall, M. Lentze, 2002, Journal of pediatric gastroenterology and nutrition.

Micronutrient status in phenylketonuria.

A. Macdonald, J. Rocha, M. Rijn, 2013, Molecular genetics and metabolism.

Hair zinc and copper in Indonesian infants.

P. Kolsteren, P. Traissac, P. Goyens, 1998, Asia Pacific journal of clinical nutrition.

Main issues in micronutrient supplementation in phenylketonuria.

A. Macdonald, J. Rocha, M. Rijn, 2013, Molecular genetics and metabolism.

A Belgian consensus-statement on growing-up milks for children 12–36 months old

J. Rigo, Y. Vandenplas, D. Brasseur, 2014, European Journal of Pediatrics.

Nutritional Status of Children Hospitalized for Parapneumonic Effusion

Y. Vandenplas, J. De Schepper, A. Malfroot, 2014, PloS one.

Intestinal Parasites In Children of Cochabamba – Bolivia

F. Jacobs, P. Goyens, I. Alvarez, 2020 .

Growth, nutritional status, and signs of rickets in 0–5-year-old children in a Kashin–Beck disease endemic area of Central Tibet

P. Bally, M. Dramaix-Wilmet, P. Goyens, 2012, European Journal of Pediatrics.

Nutritional issues in KBD endemic rural areas.

P. Bally, F. Malaisse, P. Goyens, 2008 .

Neurocognitive outcome and mental health in children with tyrosinemia type 1 and phenylketonuria: A comparison between two genetic disorders affecting the same metabolic pathway

C. Hollak, F. Eyskens, D. Cassiman, 2022, Journal of inherited metabolic disease.

Early treatment of a child with NAGS deficiency using N-carbamyl glutamate results in a normal neurological outcome

A. Jansen, G. Martens, L. Meirleir, 2014, European Journal of Pediatrics.

Selenium deficiency as a possible factor in the pathogenesis of myxoedematous endemic cretinism.

J. Dumont, J. Golstein, P. Goyens, 1987, Acta endocrinologica.

Pitfalls of ketogenic diet in a neonate.

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

Selenium and the thyroid: how the relationship was established.

J. Dumont, B. Corvilain, F. Lamy, 1993, The American journal of clinical nutrition.

A propos des champignons comestibles du Tibet centro-austral (R.P.Chine) About South-Central Tibet edible mushrooms (P.R. China)

M. Hinsenkamp, A. Kesel, G. Lognay, 2007 .

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

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

Kashin-Beck Disease: evaluation of mineral intake in young Tibetan children from endemic areas

G. Lognay, P. Maesen, P. Goyens, 2010 .

Humanitarian Aid and Health Services in Eastern Kivu, Zaire: Collaboration or competition?

P. Hennart, D. Porignon, P. Goyens, 1996 .

Antigenic variation of vibrio el Tor during an epidemic in Kivu.

J. Colaert, P. Goyens, C. Schyns, 1978, Annales de la Societe belge de medecine tropicale.

Treatment of esophageal caustic injuries: experience with high-dose dexamethasone

P. Goyens, S. Cadranel, P. Rodesch, 1993, Pediatric Surgery International.

Achalasia-alacrima-ACTH insensitivity syndrome (Triple-A-syndrome).

C. Christophe, N. Perlmutter, C. Dugardeyn, 1993, Journal belge de radiologie.

Copper deficiency in infants with active celiac disease.

D. Brasseur, P. Goyens, S. Cadranel, 1985, Journal of pediatric gastroenterology and nutrition.

Familial adrenocortiocotropin unresponsiveness associated With alacrima and achalasia: Biochemical and molecular studies in two siblings with clincial heterogeneity

G. Chrousos, C. Heinrichs, C. Dugardeyn, 1995, European Journal of Pediatrics.

P. Goyens, P. Bourdoux, C. de Laet, 2005, Clinical chemistry.

More training and awareness are needed to improve the recognition of undernutrition in hospitalised children

Y. Vandenplas, J. De Schepper, P. Bontems, 2015, Acta paediatrica.

Neurocognitive outcome in tyrosinemia type 1 patients compared to healthy controls

F. Eyskens, D. Cassiman, S. Huijbregts, 2016, Orphanet Journal of Rare Diseases.

Effect of calcium and vitamin D on growth, rickets and Kashin–Beck disease in 0‐ to 5‐year‐old children in a rural area of central Tibet

V. Maertelaer, P. Goyens, S. Rooze, 2016, Tropical medicine & international health : TM & IH.

Evaluation of nutritional care of hospitalized children in a tertiary pediatric hospital.

P. Goyens, S. Defourny, C. de Laet, 2018, Clinical nutrition ESPEN.

Is a semi-elemental diet better than a polymeric diet after congenital heart surgery?

D. Biarent, A. Willems, P. Goyens, 2019, European Journal of Pediatrics.

Rwanda: the case for research in developing countries

D. Brasseur, P. Goyens, H. Vis, 1994, The Lancet.

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

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

Neuropsychological outcome of NTBC‐treated patients with tyrosinaemia type 1

B. Dan, J. Jaeken, E. Sokal, 2011, Developmental medicine and child neurology.

Emotional and behavioral problems, quality of life and metabolic control in NTBC-treated Tyrosinemia type 1 patients

F. Eyskens, D. Cassiman, S. Huijbregts, 2019, Orphanet Journal of Rare Diseases.

Development of Risk Prediction Equations for Incident Chronic Kidney Disease

F. Eyskens, D. Cassiman, S. Huijbregts, 2020 .

Nutritional advantages of constituents of infant formulae formerly called "humanised".

P. Guesry, P. Goyens, M. Secretin, 1986, Reproduction, nutrition, developpement.

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.