Devlieger H - Search Results

1

Asplenia syndrome and isolated total anomalous pulmonary venous connection in siblings.

Devriendt K, Casaer A, Van Cauter A, de Zegher F, Dumoulin M, Gewillig M, Devlieger H. Devriendt K, et al. Among authors: devlieger h. Eur J Pediatr. 1994 Oct;153(10):712-4. doi: 10.1007/BF01954484. Eur J Pediatr. 1994. PMID: 7813525

2

Pseudo-Bartter syndrome in a neonate on prostaglandin infusion.

Vanhaesebrouck S, Allegaert K, Vanhole C, Devlieger H, Gewillig M, Proesmans W. Vanhaesebrouck S, et al. Among authors: devlieger h. Eur J Pediatr. 2003 Sep;162(9):569-71. doi: 10.1007/s00431-003-1201-3. Epub 2003 Jun 17. Eur J Pediatr. 2003. PMID: 12811550

3

Dopamine suppresses thyroid-stimulating hormone secretion in neonatal hypothyroidism.

de Zegher F, Van den Bershe G, Dumoulin M, Gewillig M, Daenen W, Devlieger H. de Zegher F, et al. Among authors: devlieger h. Acta Paediatr. 1995 Feb;84(2):213-4. doi: 10.1111/j.1651-2227.1995.tb13614.x. Acta Paediatr. 1995. PMID: 7756813

4

Agenesis of corpus callosum and anophthalmia in the asplenia syndrome. A recognisable association?

Devriendt K, Naulaers G, Matthijs G, Van Houdt K, Devlieger H, Gewillig M, Fryns JP. Devriendt K, et al. Among authors: devlieger h. Ann Genet. 1997;40(1):14-7. Ann Genet. 1997. PMID: 9150845

5

Submicroscopic deletion in chromosome 22q11 in trizygous triplet siblings and their father. Clinical variability of 22q11 deletion.

Devriendt K, Van Hoestenberghe R, Van Hole C, Devlieger H, Gewillig M, Moerman P, Van den Berghe H, Fryns JP. Devriendt K, et al. Among authors: devlieger h. Clin Genet. 1997 Apr;51(4):246-9. doi: 10.1111/j.1399-0004.1997.tb02463.x. Clin Genet. 1997. PMID: 9184246

6

Management with a staged approach of the premature hydropic fetus due to complete congenital heart block.

Deloof E, Devlieger H, Van Hoestenberghe R, Van den berghe K, Daenen W, Gewillig M. Deloof E, et al. Among authors: devlieger h. Eur J Pediatr. 1997 Jul;156(7):521-3. doi: 10.1007/s004310050652. Eur J Pediatr. 1997. PMID: 9243231

7

Alobar holoprosencephaly, diabetes insipidus and coloboma without craniofacial abnormalities: a case report.

Van Gool S, de Zegher F, de Vries LS, Vanderschueren-Lodeweyckx M, Devlieger H, Casaer P, Eggermont E. Van Gool S, et al. Among authors: devlieger h. Eur J Pediatr. 1990 Jun;149(9):621-2. doi: 10.1007/BF02034747. Eur J Pediatr. 1990. PMID: 2373111

8

Diaphragmatic hernia in Denys-Drash syndrome.

Devriendt K, Deloof E, Moerman P, Legius E, Vanhole C, de Zegher F, Proesmans W, Devlieger H. Devriendt K, et al. Among authors: devlieger h. Am J Med Genet. 1995 May 22;57(1):97-101. doi: 10.1002/ajmg.1320570120. Am J Med Genet. 1995. PMID: 7645607

9

Properties of growth hormone and prolactin hypersecretion by the human infant on the day of birth.

de Zegher F, Devlieger H, Veldhuis JD. de Zegher F, et al. Among authors: devlieger h. J Clin Endocrinol Metab. 1993 May;76(5):1177-81. doi: 10.1210/jcem.76.5.8496309. J Clin Endocrinol Metab. 1993. PMID: 8496309

10

Proteinuria in a patient with the diaphragmatic hernia-hypertelorism-myopia-deafness syndrome: further evidence that the facio-oculo-acoustico-renal syndrome represents the same entity.

Devriendt K, Standaert L, Van Hole C, Devlieger H, Fryns JP. Devriendt K, et al. Among authors: devlieger h. J Med Genet. 1998 Jan;35(1):70-1. doi: 10.1136/jmg.35.1.70. J Med Genet. 1998. PMID: 9475100 Free PMC article.

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