Heinrichs C - Search Results

1

Craniosynostosis in the Ullrich-Turner syndrome.

Heinrichs C, Elmer C, Derasse M, Perlmutter N, Vamos E. Heinrichs C, et al. Am J Med Genet. 1991 Aug 1;40(2):252. doi: 10.1002/ajmg.1320400227. Am J Med Genet. 1991. PMID: 1760044 No abstract available.

2

[Nanism with short limbs, dysmorphism, renal dysplasia, growth hormone deficiency with pituitary hypoplasia and psychomotor delay: a new syndrome?].

Elmer C, Van Vliet G, Heinrichs C, Toppet M, Christophe C, Perlmutter-Cremer N, Vamos E. Elmer C, et al. Among authors: heinrichs c. J Genet Hum. 1989 Dec;37(4-5):367-72. J Genet Hum. 1989. PMID: 2635713 French.

3

Hypergonadotropic hypogonadism in a boy with Fanconi anemia with growth hormone deficiency and pituitary stalk interruption.

Massa GG, Heinrichs C, Vamos E, Van Vliet G. Massa GG, et al. Among authors: heinrichs c. J Pediatr. 2002 Feb;140(2):277. doi: 10.1067/mpd.2002.119174. J Pediatr. 2002. PMID: 11865289 No abstract available.

4

MRI in seven cases of Rathke's cleft cyst in infants and children.

Christophe C, Flamant-Durand J, Hanquinet S, Heinrichs C, Raftopoulos C, Sariban E, Segebarth C, Perlmutter N. Christophe C, et al. Among authors: heinrichs c. Pediatr Radiol. 1993;23(2):79-82. doi: 10.1007/BF02012389. Pediatr Radiol. 1993. PMID: 8516048

5

[Contribution of MRI in 5 cases of central diabetes insipidus].

Christophe C, Balériaux D, Hanquinet S, Heinrichs C, Sariban E, Segebarth C, Van Vliet G, Perlmutter N. Christophe C, et al. Among authors: heinrichs c. Pediatrie. 1990;45(7-8):505-10. Pediatrie. 1990. PMID: 2170928 French.

6

Growth failure, encephalopathy, and endocrine dysfunctions in two siblings, one with 5-oxoprolinase deficiency.

Cohen LH, Vamos E, Heinrichs C, Toppet M, Courtens W, Kumps A, Mardens Y, Carlsson B, Grillner L, Larsson A. Cohen LH, et al. Among authors: heinrichs c. Eur J Pediatr. 1997 Dec;156(12):935-8. doi: 10.1007/s004310050746. Eur J Pediatr. 1997. PMID: 9453376

7

Screening for Turner's syndrome by chromosome analysis of all girls with short stature.

Massa GG, Verlinde V, Heinrichs C; Belgian Study Group of Pediatric Endocrinology. Massa GG, et al. Among authors: heinrichs c. J Pediatr. 2002 Jan;140(1):141-2. doi: 10.1067/mpd.2002.119173. J Pediatr. 2002. PMID: 11838440 No abstract available.

8

Congenital central isolated hypothyroidism caused by a homozygous mutation in the TSH-beta subunit gene.

Heinrichs C, Parma J, Scherberg NH, Delange F, Van Vliet G, Duprez L, Bourdoux P, Bergmann P, Vassart G, Refetoff S. Heinrichs C, et al. Thyroid. 2000 May;10(5):387-91. doi: 10.1089/thy.2000.10.387. Thyroid. 2000. PMID: 10884185

9

Fetal hypopituitarism: perinatal endocrine and morphological studies in two cases.

Heinrichs C, de Zegher F, Vansnick F, Vokaer A, Christophe C, Frankenne F. Heinrichs C, et al. Acta Paediatr. 1994 Apr;83(4):448-51. doi: 10.1111/j.1651-2227.1994.tb18143.x. Acta Paediatr. 1994. PMID: 8025410

10

Growth-promoting effect of growth hormone and low dose ethinyl estradiol in girls with Turner's syndrome.

Vanderschueren-Lodeweyckx M, Massa G, Maes M, Craen M, van Vliet G, Heinrichs C, Malvaux P. Vanderschueren-Lodeweyckx M, et al. Among authors: heinrichs c. J Clin Endocrinol Metab. 1990 Jan;70(1):122-6. doi: 10.1210/jcem-70-1-122. J Clin Endocrinol Metab. 1990. PMID: 2294126 Clinical Trial.

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