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Items: 1 to 20 of 84

1.

Anatomical, animal, and cellular evidence for Zika-induced pathogenesis of fetal microcephaly.

Wang JZ, Guo XH, Xu DG.

Brain Dev. 2016 Nov 19. pii: S0387-7604(16)30181-4. doi: 10.1016/j.braindev.2016.10.012. [Epub ahead of print] Review.

PMID:
27876396
2.

Zika Virus Infection and Microcephaly: Evidence for a Causal Link.

Wang JN, Ling F.

Int J Environ Res Public Health. 2016 Oct 20;13(10). pii: E1031. Review.

3.

Available Evidence of Association between Zika Virus and Microcephaly.

Wu J, Huang DY, Ma JT, Ma YH, Hu YF.

Chin Med J (Engl). 2016 5th Oct;129(19):2347-56. doi: 10.4103/0366-6999.190672. Review.

4.

The genetic epidemiology of the form of microcephaly ascribed to mutation at the WDR62 locus.

Stark AE.

Ann Transl Med. 2016 Aug;4(15):281. doi: 10.21037/atm.2016.07.08. Review.

5.

Microcephaly and Zika virus: a clinical and epidemiological analysis of the current outbreak in Brazil.

Nunes ML, Carlini CR, Marinowic D, Neto FK, Fiori HH, Scotta MC, Zanella PL, Soder RB, da Costa JC.

J Pediatr (Rio J). 2016 May-Jun;92(3):230-40. doi: 10.1016/j.jped.2016.02.009. Review.

6.

Zika virus and autoimmunity: From microcephaly to Guillain-Barré syndrome, and beyond.

Lucchese G, Kanduc D.

Autoimmun Rev. 2016 Aug;15(8):801-8. doi: 10.1016/j.autrev.2016.03.020. Review.

PMID:
27019049
7.

Mandibulofacial Dysostosis with Microcephaly: Mutation and Database Update.

Huang L, Vanstone MR, Hartley T, Osmond M, Barrowman N, Allanson J, Baker L, Dabir TA, Dipple KM, Dobyns WB, Estrella J, Faghfoury H, Favaro FP, Goel H, Gregersen PA, Gripp KW, Grix A, Guion-Almeida ML, Harr MH, Hudson C, Hunter AG, Johnson J, Joss SK, Kimball A, Kini U, Kline AD, Lauzon J, Lildballe DL, López-González V, Martinezmoles J, Meldrum C, Mirzaa GM, Morel CF, Morton JE, Pyle LC, Quintero-Rivera F, Richer J, Scheuerle AE, Schönewolf-Greulich B, Shears DJ, Silver J, Smith AC, Temple IK; UCLA Clinical Genomics Center., van de Kamp JM, van Dijk FS, Vandersteen AM, White SM, Zackai EH, Zou R; Care4Rare Canada Consortium., Bulman DE, Boycott KM, Lines MA.

Hum Mutat. 2016 Feb;37(2):148-54. doi: 10.1002/humu.22924. Review.

PMID:
26507355
8.

Measuring head circumference: Update on infant microcephaly.

Harris SR.

Can Fam Physician. 2015 Aug;61(8):680-4. Review.

9.

What next-generation sequencing (NGS) technology has enabled us to learn about primary autosomal recessive microcephaly (MCPH).

Morris-Rosendahl DJ, Kaindl AM.

Mol Cell Probes. 2015 Oct;29(5):271-81. doi: 10.1016/j.mcp.2015.05.015. Review.

PMID:
26050940
10.

Molecular genetics of human primary microcephaly: an overview.

Faheem M, Naseer MI, Rasool M, Chaudhary AG, Kumosani TA, Ilyas AM, Pushparaj P, Ahmed F, Algahtani HA, Al-Qahtani MH, Saleh Jamal H.

BMC Med Genomics. 2015;8 Suppl 1:S4. doi: 10.1186/1755-8794-8-S1-S4. Review.

11.

Molecular and cellular basis of autosomal recessive primary microcephaly.

Barbelanne M, Tsang WY.

Biomed Res Int. 2014;2014:547986. doi: 10.1155/2014/547986. Review.

12.

Congenital microcephaly and chorioretinopathy due to de novo heterozygous KIF11 mutations: five novel mutations and review of the literature.

Mirzaa GM, Enyedi L, Parsons G, Collins S, Medne L, Adams C, Ward T, Davitt B, Bicknese A, Zackai E, Toriello H, Dobyns WB, Christian S.

Am J Med Genet A. 2014 Nov;164A(11):2879-86. doi: 10.1002/ajmg.a.36707. Review.

13.

Mandibulofacial Dysostosis with Microcephaly.

Lines M, Hartley T, Boycott KM.

In: Pagon RA, Adam MP, Ardinger HH, Wallace SE, Amemiya A, Bean LJH, Bird TD, Ledbetter N, Mefford HC, Smith RJH, Stephens K, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2017.
2014 Jul 3.

14.

Genetic disorders associated with postnatal microcephaly.

Seltzer LE, Paciorkowski AR.

Am J Med Genet C Semin Med Genet. 2014 Jun;166C(2):140-55. doi: 10.1002/ajmg.c.31400. Review.

PMID:
24839169
15.

Congenital microcephaly.

Alcantara D, O'Driscoll M.

Am J Med Genet C Semin Med Genet. 2014 Jun;166C(2):124-39. doi: 10.1002/ajmg.c.31397. Review.

PMID:
24816482
16.

Diagnostic approach to microcephaly in childhood: a two-center study and review of the literature.

von der Hagen M, Pivarcsi M, Liebe J, von Bernuth H, Didonato N, Hennermann JB, Bührer C, Wieczorek D, Kaindl AM.

Dev Med Child Neurol. 2014 Aug;56(8):732-41. doi: 10.1111/dmcn.12425. Review.

17.

Emerging roles of MCPH1: expedition from primary microcephaly to cancer.

Venkatesh T, Suresh PS.

Eur J Cell Biol. 2014 Mar;93(3):98-105. doi: 10.1016/j.ejcb.2014.01.005. Review.

PMID:
24560403
18.

Thin genu of the corpus callosum points to mutation in FOXG1 in a child with acquired microcephaly, trigonocephaly, and intellectual developmental disorder: a case report and review of literature.

De Bruyn C, Vanderhasselt T, Tanyalçin I, Keymolen K, Van Rompaey KL, De Meirleir L, Jansen AC.

Eur J Paediatr Neurol. 2014 May;18(3):420-6. doi: 10.1016/j.ejpn.2013.11.010. Review.

PMID:
24388699
19.

Microcephaly-Capillary Malformation Syndrome.

Carter MT, Mirzaa G, McDonell LM, Boycott KM.

In: Pagon RA, Adam MP, Ardinger HH, Wallace SE, Amemiya A, Bean LJH, Bird TD, Ledbetter N, Mefford HC, Smith RJH, Stephens K, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2017.
2013 Dec 12.

20.

Genetic causes of microcephaly and lessons for neuronal development.

Gilmore EC, Walsh CA.

Wiley Interdiscip Rev Dev Biol. 2013 Jul;2(4):461-78. doi: 10.1002/wdev.89. Review.

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