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Practice parameter: Evaluation of the child with microcephaly (an evidence-based review): report of the Quality Standards Subcommittee of the American Academy of Neurology and the Practice Committee of the Child Neurology Society.
Ashwal S, Michelson D, Plawner L, Dobyns WB; Quality Standards Subcommittee of the American Academy of Neurology and the Practice Committee of the Child Neurology Society.
Neurology. 2009 Sep 15;73(11):887-97.PMID: 19752457 [PubMed - indexed for MEDLINE]Related articles
Partial trisomy 19p13.3 and partial monosomy 1p36.3: Clinical report and a literature review.
Puvabanditsin S, Garrow E, Brandsma E, Savla J, Kunjumon B, Gadi I.
Am J Med Genet A. 2009 Aug;149A(8):1782-5. Review.PMID: 19610110 [PubMed - indexed for MEDLINE]Related articles
A 649 kb microduplication in 1p34.1, including POMGNT1, in a patient with microcephaly, coloboma and laryngomalacia; and a review of the literature.
Hanemaaijer N, Dijkhuizen T, Haadsma M, Boeve M, Boon M, Hordijk R, Kok K, Sikkema-Raddatz B, van Ravenswaaij-Arts CM.
Eur J Med Genet. 2009 Mar-Jun;52(2-3):116-9. Review.PMID: 19452620 [PubMed - indexed for MEDLINE]Related articles
Reviewing the evidence for mycophenolate mofetil as a new teratogen: case report and review of the literature.
Anderka MT, Lin AE, Abuelo DN, Mitchell AA, Rasmussen SA.
Am J Med Genet A. 2009 Jun;149A(6):1241-8. Review.PMID: 19441125 [PubMed - indexed for MEDLINE]Related articles
Microcephaly: a radiological review.
Tarrant A, Garel C, Germanaud D, de Villemeur TB, Mignot C, Lenoir M, le Pointe HD.
Pediatr Radiol. 2009 Aug;39(8):772-80; quiz 888-9. Epub 2009 May 13. Review.PMID: 19437006 [PubMed - indexed for MEDLINE]Related articles
Post-natal investigations: management and prognosis for fetuses with CNS anomalies identified in utero excluding neurosurgical problems.
Mighell AS, Johnstone ED, Levene M.
Prenat Diagn. 2009 Apr;29(4):442-9. Review.PMID: 19333959 [PubMed - indexed for MEDLINE]Related articles
The expanding phenotype of GLUT1-deficiency syndrome.
Brockmann K.
Brain Dev. 2009 Aug;31(7):545-52. Epub 2009 Mar 21. Review.PMID: 19304421 [PubMed - indexed for MEDLINE]Related articles
Genetic imprinting: the paradigm of Prader-Willi and Angelman syndromes.
Gurrieri F, Accadia M.
Endocr Dev. 2009;14:20-8. Epub 2009 Feb 27. Review.PMID: 19293572 [PubMed - indexed for MEDLINE]Related articles
Treatment of congenital cytomegalovirus infection: implications for future therapeutic strategies.
Nassetta L, Kimberlin D, Whitley R.
J Antimicrob Chemother. 2009 May;63(5):862-7. Epub 2009 Mar 14. Review.PMID: 19287011 [PubMed - indexed for MEDLINE]Related articles
Mammalian sperm quality and aromatase expression.
Carreau S, Delalande C, Galeraud-Denis I.
Microsc Res Tech. 2009 Aug;72(8):552-7. Review.PMID: 19263495 [PubMed - indexed for MEDLINE]Related articles
Abnormalities of the foetal cerebral cortex.
Toi A, Chitayat D, Blaser S.
Prenat Diagn. 2009 Apr;29(4):355-71. Review.PMID: 19235759 [PubMed - indexed for MEDLINE]Related articles
Disorders of biopterin metabolism.
Longo N.
J Inherit Metab Dis. 2009 Jun;32(3):333-42. Epub 2009 Feb 9. Review. Erratum in: J Inherit Metab Dis. 2009 Jun;32(3):457. PMID: 19234759 [PubMed - indexed for MEDLINE]Related articles
Primary hypogonadism, partial alopecia, and Mullerian hypoplasia: report of a third family and review.
Tatar A, Ocak Z, Tatar A, Yesilyurt A, Borekci B, Oztas S.
Am J Med Genet A. 2009 Mar;149A(3):501-4. Review.PMID: 19213036 [PubMed - indexed for MEDLINE]Related articles
Interstitial deletion 2p11.2-p12: report of a patient with mental retardation and review of the literature.
Tzschach A, Graul-Neumann LM, Konrat K, Richter R, Ebert G, Ullmann R, Neitzel H.
Am J Med Genet A. 2009 Feb;149A(2):242-5. Review.PMID: 19161151 [PubMed - indexed for MEDLINE]Related articles
Aicardi-Goutieres syndrome.
Orcesi S, La Piana R, Fazzi E.
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The Fanconi anemia/BRCA gene network in zebrafish: embryonic expression and comparative genomics.
Titus TA, Yan YL, Wilson C, Starks AM, Frohnmayer JD, Bremiller RA, Cañestro C, Rodriguez-Mari A, He X, Postlethwait JH.
Mutat Res. 2009 Jul 31;668(1-2):117-32. Epub 2008 Dec 3. Review.PMID: 19101574 [PubMed - indexed for MEDLINE]Related articles
Radiation biology for pediatric radiologists.
Hall EJ.
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Neonatal manifestation of multiple sulfatase deficiency.
Busche A, Hennermann JB, Bürger F, Proquitté H, Dierks T, von Arnim-Baas A, Horn D.
Eur J Pediatr. 2009 Aug;168(8):969-73. Epub 2008 Dec 10. Review.PMID: 19066960 [PubMed - indexed for MEDLINE]Related articles
Cytomegalovirus-related fetal brain lesions: comparison between targeted ultrasound examination and magnetic resonance imaging.
Benoist G, Salomon LJ, Mohlo M, Suarez B, Jacquemard F, Ville Y.
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Nijmegen breakage syndrome and functions of the responsible protein, NBS1.
Antoccia A, Kobayashi J, Tauchi H, Matsuura S, Komatsu K.
Genome Dyn. 2006;1:191-205. Review.PMID: 18724061 [PubMed - indexed for MEDLINE]Related articles
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