Massa G - Search Results

1

46,XX/46,XX,del(20)(pter-->p12.2) mosaicism limited to fibroblasts associated with MCA/MR and severe growth deficit.

Fryns JP, Kleczkowska A, Decock P, Massa G, van den Berghe H. Fryns JP, et al. Among authors: massa g. Ann Genet. 1992;35(4):234-6. Ann Genet. 1992. PMID: 1296522

2

Deletion of the short arm of the X chromosome: a hereditary form of Turner syndrome.

Massa G, Vanderschueren-Lodeweyckx M, Fryns JP. Massa G, et al. Eur J Pediatr. 1992 Dec;151(12):893-4. doi: 10.1007/BF01954124. Eur J Pediatr. 1992. PMID: 1473542

3

Intelligence, behaviour and psychosocial development in Turner syndrome. A cross-sectional study of 50 pre-adolescent and adolescent girls (4-20 years).

Swillen A, Fryns JP, Kleczkowska A, Massa G, Vanderschueren-Lodeweyckx M, Van den Berghe H. Swillen A, et al. Among authors: massa g. Genet Couns. 1993;4(1):7-18. Genet Couns. 1993. PMID: 8471226

4

Opposite effects of growth hormone and estrogens on the pregnancy zone protein serum levels in children and adolescents.

Devriendt K, Massa G, de Zegher F, Vanderschueren-Lodeweyckx M, Cassiman JJ, Van den Berghe H, Marynen P. Devriendt K, et al. Among authors: massa g. Acta Endocrinol (Copenh). 1993 Apr;128(4):334-8. doi: 10.1530/acta.0.1280334. Acta Endocrinol (Copenh). 1993. PMID: 8498151

5

Tumor spectrum in children with Noonan syndrome and SOS1 or RAF1 mutations.

Denayer E, Devriendt K, de Ravel T, Van Buggenhout G, Smeets E, Francois I, Sznajer Y, Craen M, Leventopoulos G, Mutesa L, Vandecasseye W, Massa G, Kayserili H, Sciot R, Fryns JP, Legius E. Denayer E, et al. Among authors: massa g. Genes Chromosomes Cancer. 2010 Mar;49(3):242-52. doi: 10.1002/gcc.20735. Genes Chromosomes Cancer. 2010. PMID: 19953625

6

Growth hormone deficiency in a girl with the Cohen syndrome.

Massa G, Dooms L, Vanderschueren-Lodeweyckx M. Massa G, et al. J Med Genet. 1991 Jan;28(1):48-50. doi: 10.1136/jmg.28.1.48. J Med Genet. 1991. PMID: 1999833 Free PMC article.

7

Arthrogryposis multiplex congenita associated with lissencephaly: a case report.

Massa G, Casaer P, Ceulemans B, Van Eldere S. Massa G, et al. Neuropediatrics. 1988 Feb;19(1):24-6. doi: 10.1055/s-2008-1052396. Neuropediatrics. 1988. PMID: 3362309

8

Spondyloepiphyseal dysplasia tarda in Turner syndrome.

Massa G, Vanderschueren-Lodeweyckx M. Massa G, et al. Acta Paediatr Scand. 1989 Nov;78(6):971-4. doi: 10.1111/j.1651-2227.1989.tb11189.x. Acta Paediatr Scand. 1989. PMID: 2603728

9

A de-novo 15q24.2 deletion involving SIN3A is associated with emotional, behavioural, motor problems and hypersensitivity in a girl with above average intelligence and typical facial features.

Sleyp Y, Swillen A, Van Den Bogaert K, Massa G, Aerssens P, Peeters H. Sleyp Y, et al. Among authors: massa g. Clin Dysmorphol. 2020 Oct;29(4):210-213. doi: 10.1097/MCD.0000000000000337. Clin Dysmorphol. 2020. PMID: 32639238 No abstract available.

10

Hyperthyroidism accelerates growth in Turner's syndrome.

Massa G, de Zegher F, Dooms L, Vanderschueren-Lodeweyckx M. Massa G, et al. Acta Paediatr. 1992 Apr;81(4):362-4. doi: 10.1111/j.1651-2227.1992.tb12245.x. Acta Paediatr. 1992. PMID: 1606402

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