Frijns JP - Search Results

1

Ehlers-Danlos syndrome type IV: a heterogeneous disease.

Lauwers G, Nevelsteen A, Daenen G, Lacroix H, Suy R, Frijns JP. Lauwers G, et al. Among authors: frijns jp. Ann Vasc Surg. 1997 Mar;11(2):178-82. doi: 10.1007/s100169900031. Ann Vasc Surg. 1997. PMID: 9181775

2

The Holt-Oram syndrome: radiological approach.

Penne D, Delanote G, Breysem L, Frijns JP, Smet MH, Baert AL. Penne D, et al. Among authors: frijns jp. J Belge Radiol. 1997 Jun;80(3):118-9. J Belge Radiol. 1997. PMID: 9260393

3

Syndrome of Hajdu-Cheney: three case reports of orofacial interest.

Vingerhoedt E, Bailleul-Forestier I, Fellus P, Schoenaers J, Frijns JP, Carels C. Vingerhoedt E, et al. Among authors: frijns jp. Cleft Palate Craniofac J. 2010 Nov;47(6):645-53. doi: 10.1597/09-030. Epub 2010 Mar 1. Cleft Palate Craniofac J. 2010. PMID: 20500061

4

Unique cause of renovascular hypertension: melorheostosis associated with a malformation of the renal arteries.

de Goede E, Fagard R, Frijns JP. de Goede E, et al. Among authors: frijns jp. J Hum Hypertens. 1996 Jan;10(1):57-9. J Hum Hypertens. 1996. PMID: 8642192

5

The psychopathological phenotype of velo-cardio-facial syndrome.

Vogels A, Verhoeven WM, Tuinier S, DeVriendt K, Swillen A, Curfs LM, Frijns JP. Vogels A, et al. Among authors: frijns jp. Ann Genet. 2002 Apr-Jun;45(2):89-95. doi: 10.1016/s0003-3995(02)01114-0. Ann Genet. 2002. PMID: 12119217 Review.

6

The velo-cardio-facial syndrome: the otorhinolaryngeal manifestations and implications.

Vantrappen G, Rommel N, Cremers CW, Devriendt K, Frijns JP. Vantrappen G, et al. Among authors: frijns jp. Int J Pediatr Otorhinolaryngol. 1998 Oct 2;45(2):133-41. doi: 10.1016/s0165-5876(98)00067-6. Int J Pediatr Otorhinolaryngol. 1998. PMID: 9849681 Review.

7

3-Phosphoglycerate dehydrogenase deficiency and 3-phosphoserine phosphatase deficiency: inborn errors of serine biosynthesis.

Jaeken J, Detheux M, Van Maldergem L, Frijns JP, Alliet P, Foulon M, Carchon H, Van Schaftingen E. Jaeken J, et al. Among authors: frijns jp. J Inherit Metab Dis. 1996;19(2):223-6. doi: 10.1007/BF01799435. J Inherit Metab Dis. 1996. PMID: 8739971 No abstract available.

8

Microduplication 22q11.2: a description of the clinical, developmental and behavioral characteristics during childhood.

Van Campenhout S, Devriendt K, Breckpot J, Frijns JP, Peeters H, Van Buggenhout G, Van Esch H, Maes B, Swillen A. Van Campenhout S, et al. Among authors: frijns jp. Genet Couns. 2012;23(2):135-48. Genet Couns. 2012. PMID: 22876571

9

Conductive hearing loss in the tricho-rhino-phalangeal syndrome (TRP II) or in the Langer-Giedion syndrome.

Vantrappen G, Feenstra L, Frijns JP. Vantrappen G, et al. Among authors: frijns jp. Am J Med Genet. 1997 Oct 31;72(3):372-3. doi: 10.1002/(sici)1096-8628(19971031)72:3<372::aid-ajmg25>3.0.co;2-p. Am J Med Genet. 1997. PMID: 9332674 No abstract available.

10

Neuropsychopathology in 7 Patients with the 22q13 Deletion Syndrome: Presence of Bipolar Disorder and Progressive Loss of Skills.

Denayer A, Van Esch H, de Ravel T, Frijns JP, Van Buggenhout G, Vogels A, Devriendt K, Geutjens J, Thiry P, Swillen A. Denayer A, et al. Among authors: frijns jp. Mol Syndromol. 2012 Jun;3(1):14-20. doi: 10.1159/000339119. Epub 2012 May 16. Mol Syndromol. 2012. PMID: 22855650 Free PMC article.

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