References of "Pieltain, Catherine"
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See detailElectrolyte and mineral homeostasis after optimizing early macronutrient intakes in VLBW infants on parenteral nutrition
SENTERRE, Thibault ULg; Abu Zahirah, Ibrahim; PIELTAIN, Catherine ULg et al

in Journal of Pediatric Gastroenterology and Nutrition (2015), 6(14), 491-498

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See detailCerebellar hemorrhage : a rare condition in the term infant
MERINDOL, Ninon; BROUX, Isabelle ULg; DECORTIS, Thierry et al

Poster (2015)

Cerebellar hemorrhage is a rare condition in full-term newborns. Early diagnosis based on the identification of risk factors, particular clinical signs and correct medical imaging is primordial to ... [more ▼]

Cerebellar hemorrhage is a rare condition in full-term newborns. Early diagnosis based on the identification of risk factors, particular clinical signs and correct medical imaging is primordial to optimize the immediate treatment and to assess the long term prognosis. [less ▲]

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See detailIs early aggressive feeding dangerous for extremely low birth weight infants?
Blecic, Anne-Sophie; Delbos, Marion; RIGO, Vincent ULg et al

in Tijdschrift van de Belgische Kinderarts = Journal du Pédiatre Belge (2015), 17(1), 83

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See detailCOMMENT J’EXPLORE ET TRAITE UNE THROMBOSE VEINEUSE RÉNALE NÉONATALE : à propos d’un cas
Tribolet, S.; DRESSE, Marie-Françoise ULg; Lombet, J. et al

in Revue Médicale de Liège (2014), 69(4), 169-174

Neonatal renal vein thrombosis is a rare condition. The present case is rather unfrequent and particularly educative since it shows the complete diagnostic triad including hematuria, flank mass and ... [more ▼]

Neonatal renal vein thrombosis is a rare condition. The present case is rather unfrequent and particularly educative since it shows the complete diagnostic triad including hematuria, flank mass and thrombocytopenia. The diagnosis relies on the demonstration, by Doppler ultrasound, of an obstructed renal venous bed. The investigation is completed by a platelet count and the determination of the prothrombin time, of the activated partial thromboplastin time as well as of the concentration of fibrinogen. The screening also includes the search for a possible etiology, such as a deficiency in coagulation proteins, the presence of antiphospholipid antibodies or of a genetic mutation of one of the coagulation factors. Since there exist no evidence based guidelines for the management of the disease, we will discuss the diagnosis and treatment in relation with the published literature. [less ▲]

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See detailPrematurity and bone health
PIELTAIN, Catherine ULg; de HALLEUX, Virginie ULg; SENTERRE, Thibault ULg et al

in World Review of Nutrition and Dietetics (2013), 106

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See detailCalcium and Phosphorus Homeostasis: Pathophysiology
RIGO, Jacques ULg; PIELTAIN, Catherine ULg; VIELLEVOYE, Renaud ULg et al

in BUONOCORE, Giuseppe; BRACCI, Rodolfo; WEINDLING, Michael (Eds.) Neonatology. A practical approach to neonatal diseases. (2012)

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See detailNutrition du prématuré après la sortie: lait, vitamines, fer, diversification
Rigo, Jacques ULg; Habibi, Fakher; Senterre, Thibault ULg et al

in Archives Françaises de Pédiatrie (2010), 17

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See detailCord blood transplantation in a child with Pearson's disease.
Hoyoux, Claire; Dresse, Marie-Françoise ULg; Robinet, Sébastien ULg et al

in Pediatric Blood & Cancer (2008), 51(4), 566

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See detailLe syndrome de Prader Willi: intérêt d'une prise en charge pluridisciplinaire
Salmon, C.; Gaillez, Stephanie ULg; Pieltain, Catherine ULg et al

in Revue Médicale de Liège (2006), 61(7-8, Jul-Aug), 593-599

Prader Willi syndrome can be viewed as a physiopathological model of obesity. Such patients deserve specific management, preferably in a multidisciplinary setting. The paper reports on 6 patients followed ... [more ▼]

Prader Willi syndrome can be viewed as a physiopathological model of obesity. Such patients deserve specific management, preferably in a multidisciplinary setting. The paper reports on 6 patients followed in the paediatric endocrine service at the University of Liege. [less ▲]

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See detailL'insuffisance surrénale isolée: Une cause inhabituelle d'hypoglycémie du nourrisson
Mascart, F.; Pieltain, Catherine ULg; Andoura, B. et al

in Journées annuelles de la Société Belge de Pédiatrie (1991)

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