Borghgraef M - Search Results

1

Prader-Willi syndrome and psychotic symptoms: 1. Case descriptions and genetic studies.

Clarke D, Boer H, Webb T, Scott P, Frazer S, Vogels A, Borghgraef M, Curfs LM. Clarke D, et al. Among authors: borghgraef m. J Intellect Disabil Res. 1998 Dec;42 ( Pt 6):440-50. doi: 10.1046/j.1365-2788.1998.4260440.x. J Intellect Disabil Res. 1998. PMID: 10030439

2

Prader-Willi syndrome: new insights in the behavioural and psychiatric spectrum.

Descheemaeker MJ, Vogels A, Govers V, Borghgraef M, Willekens D, Swillen A, Verhoeven W, Fryns JP. Descheemaeker MJ, et al. Among authors: borghgraef m. J Intellect Disabil Res. 2002 Jan;46(Pt 1):41-50. doi: 10.1046/j.1365-2788.2002.00354.x. J Intellect Disabil Res. 2002. PMID: 11851855

3

Strengths and weaknesses in the cognitive profile of youngsters with Prader-Willi syndrome.

Curfs LM, Wiegers AM, Sommers JR, Borghgraef M, Fryns JP. Curfs LM, et al. Among authors: borghgraef m. Clin Genet. 1991 Dec;40(6):430-4. doi: 10.1111/j.1399-0004.1991.tb03114.x. Clin Genet. 1991. PMID: 1778005

4

The Prader-Willi syndrome: a self supporting program for children, youngsters and adults.

Descheemaeker MJ, Swillen A, Plissart L, Borghgraef M, Rasenberg S, Curfs LM, Fryns JP. Descheemaeker MJ, et al. Among authors: borghgraef m. Genet Couns. 1994;5(2):199-205. Genet Couns. 1994. PMID: 7917134

5

Longitudinal changes in IQ among fragile X males: clinical evidence of more than one mutation?

Fisch GS, Shapiro LR, Simensen R, Schwartz CE, Fryns JP, Borghgraef M, Curfs LM, Howard-Peebles PN, Arinami T, Mavrou A. Fisch GS, et al. Among authors: borghgraef m. Am J Med Genet. 1992 Apr 15-May 1;43(1-2):28-34. doi: 10.1002/ajmg.1320430105. Am J Med Genet. 1992. PMID: 1605202

6

Relationship between age and IQ among fragile X males: a multicenter study.

Fisch GS, Arinami T, Froster-Iskenius U, Fryns JP, Curfs LM, Borghgraef M, Howard-Peebles PN, Schwartz CE, Simensen RJ, Shapiro LR. Fisch GS, et al. Among authors: borghgraef m. Am J Med Genet. 1991 Feb-Mar;38(2-3):481-7. doi: 10.1002/ajmg.1320380268. Am J Med Genet. 1991. PMID: 2018090

7

Intelligence and cognitive profile in the fra(X) syndrome: a longitudinal study in 18 fra(X) boys.

Curfs LM, Schreppers-Tijdink G, Wiegers A, Borghgraef M, Fryns JP. Curfs LM, et al. Among authors: borghgraef m. J Med Genet. 1989 Jul;26(7):443-6. doi: 10.1136/jmg.26.7.443. J Med Genet. 1989. PMID: 2746616 Free PMC article.

8

The 49,XXXXY syndrome: clinical and psychological findings in five patients.

Curfs LM, Schreppers-Tijdink G, Wiegers A, Borghgraef M, Fryns JP. Curfs LM, et al. Among authors: borghgraef m. J Ment Defic Res. 1990 Jun;34 ( Pt 3):277-82. doi: 10.1111/j.1365-2788.1990.tb01539.x. J Ment Defic Res. 1990. PMID: 2380984

9

Strengths and weaknesses in the cognitive profile of fra(X) patients.

Curfs LM, Borghgraef M, Wiegers A, Schreppers-Tijdink GA, Fryns JP. Curfs LM, et al. Among authors: borghgraef m. Clin Genet. 1989 Dec;36(6):405-10. Clin Genet. 1989. PMID: 2686867 Clinical Trial.

10

Autism spectrum disorder profile in neurofibromatosis type I.

Garg S, Plasschaert E, Descheemaeker MJ, Huson S, Borghgraef M, Vogels A, Evans DG, Legius E, Green J. Garg S, et al. Among authors: borghgraef m. J Autism Dev Disord. 2015 Jun;45(6):1649-57. doi: 10.1007/s10803-014-2321-5. J Autism Dev Disord. 2015. PMID: 25475362

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