Nikkels P - Search Results

1

PTEN hamartoma tumour syndrome: variability of an entity.

Merks JH, de Vries LS, Zhou XP, Nikkels P, Barth PG, Eng C, Hennekam RC. Merks JH, et al. Among authors: nikkels p. J Med Genet. 2003 Oct;40(10):e111. doi: 10.1136/jmg.40.10.e111. J Med Genet. 2003. PMID: 14569134 Free PMC article. No abstract available.

2

Congenital brainstem disconnection associated with a syrinx of the brainstem.

Barth PG, de Vries LS, Nikkels PG, Troost D. Barth PG, et al. Among authors: nikkels pg. Neuropediatrics. 2008 Feb;39(1):1-7. doi: 10.1055/s-2008-1077049. Neuropediatrics. 2008. PMID: 18504674

3

Cerebral, cerebellar, and colobomatous anomalies in three related males: Sex-linked inheritance in a newly recognized syndrome with features overlapping with Joubert syndrome.

Kroes HY, Nievelstein RJ, Barth PG, Nikkels PG, Bergmann C, Gooskens RH, Visser G, van Amstel HK, Beemer FA. Kroes HY, et al. Am J Med Genet A. 2005 Jun 15;135(3):297-301. doi: 10.1002/ajmg.a.30690. Am J Med Genet A. 2005. PMID: 15887274

4

Neonatal diffusion-weighted MR imaging: relation with histopathology or follow-up MR examination.

Roelants-van Rijn AM, Nikkels PG, Groenendaal F, van Der Grond J, Barth PG, Snoeck I, Beek FJ, de Vries LS. Roelants-van Rijn AM, et al. Among authors: nikkels pg. Neuropediatrics. 2001 Dec;32(6):286-94. doi: 10.1055/s-2001-20403. Neuropediatrics. 2001. PMID: 11870583

5

Fetus with an unusual form of nonrhizomelic chondrodysplasia punctata: case report and review.

Wessels MW, Den Hollander NJ, De Krijger RR, Nikkels PG, Brandenburg H, Hennekam R, Willems PJ. Wessels MW, et al. Am J Med Genet A. 2003 Jul 1;120A(1):97-104. doi: 10.1002/ajmg.a.20202. Am J Med Genet A. 2003. PMID: 12794700

6

Patterns of placental pathology in preterm infants with a periventricular haemorrhagic infarction: association with time of onset and clinical presentation.

Harteman JC, Nikkels PG, Kwee A, Groenendaal F, de Vries LS. Harteman JC, et al. Among authors: nikkels pg. Placenta. 2012 Oct;33(10):839-44. doi: 10.1016/j.placenta.2012.06.014. Epub 2012 Jul 25. Placenta. 2012. PMID: 22835681

7

Pontocerebellar hypoplasia type 2: a neuropathological update.

Barth PG, Aronica E, de Vries L, Nikkels PG, Scheper W, Hoozemans JJ, Poll-The BT, Troost D. Barth PG, et al. Acta Neuropathol. 2007 Oct;114(4):373-86. doi: 10.1007/s00401-007-0263-0. Epub 2007 Jul 20. Acta Neuropathol. 2007. PMID: 17641900 Free PMC article.

8

[Aneurysm of the V. magna cerebri (vein of Galen), a cause of congestive heart failure in five neonates].

van Westreenen HL, de Vries LS, Gooskens RH, Nikkels PG, Stoutenbeek P, Meijboom EJ. van Westreenen HL, et al. Among authors: nikkels pg. Ned Tijdschr Geneeskd. 2001 Aug 18;145(33):1602-5. Ned Tijdschr Geneeskd. 2001. PMID: 11534379 Dutch.

9

A known and a novel mutation in the glycine decarboxylase gene in a newborn with classic nonketotic hyperglycinemia.

Beijer P, Lichtenbelt KD, Hofstede FC, Nikkels PG, Lemmers P, de Vries LS. Beijer P, et al. Among authors: nikkels pg. Neuropediatrics. 2012 Jun;43(3):164-7. doi: 10.1055/s-0032-1313914. Epub 2012 May 19. Neuropediatrics. 2012. PMID: 22610665

10

Predictors of outcome at 2 years of age after early intrauterine growth restriction.

Torrance HL, Bloemen MC, Mulder EJ, Nikkels PG, Derks JB, de Vries LS, Visser GH. Torrance HL, et al. Among authors: nikkels pg. Ultrasound Obstet Gynecol. 2010 Aug;36(2):171-7. doi: 10.1002/uog.7627. Ultrasound Obstet Gynecol. 2010. PMID: 20217892 Free article.

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