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Clinical and genetic heterogeneity of branching enzyme deficiency (glycogenosis type IV).
Bruno C, van Diggelen OP, Cassandrini D, Gimpelev M, Giuffrè B, Donati MA, Introvini P, Alegria A, Assereto S, Morandi L, Mora M, Tonoli E, Mascelli S, Traverso M, Pasquini E, Bado M, Vilarinho L, van Noort G, Mosca F, DiMauro S, Zara F, Minetti C. Bruno C, et al. Among authors: van noort g. Neurology. 2004 Sep 28;63(6):1053-8. doi: 10.1212/01.wnl.0000138429.11433.0d. Neurology. 2004. PMID: 15452297
A congenital variant of glycogenosis type IV.
van Noort G, Straks W, Van Diggelen OP, Hennekam RC. van Noort G, et al. Among authors: van diggelen op. Pediatr Pathol. 1993 Sep-Oct;13(5):685-98. doi: 10.3109/15513819309048254. Pediatr Pathol. 1993. PMID: 8247964
Familial holoprosencephaly, heart defects, and polydactyly.
Hennekam RC, van Noort G, de la Fuente AA. Hennekam RC, et al. Among authors: van noort g. Am J Med Genet. 1991 Nov 1;41(2):258-62. doi: 10.1002/ajmg.1320410226. Am J Med Genet. 1991. PMID: 1785646 Review.
Retractile mesenteritis: to treat or not to treat.
Koornstra JJ, van Olffen GH, van Noort G. Koornstra JJ, et al. Among authors: van noort g. Hepatogastroenterology. 1997 Mar-Apr;44(14):408-10. Hepatogastroenterology. 1997. PMID: 9164510 Review.
[Pilomatrixoma often not identified as such].
Temming JF, Mastboom WJ, van Noort G. Temming JF, et al. Among authors: van noort g. Ned Tijdschr Geneeskd. 1998 Dec 5;142(49):2684-8. Ned Tijdschr Geneeskd. 1998. PMID: 10065225 Dutch.
17 results