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Items: 1 to 20 of 41

1.

Gangliosidome of human anencephaly: A high resolution multistage mass spectrometry study.

Sarbu M, Ica R, Petrut A, Vukelić Ž, Munteanu CVA, Petrescu AJ, Zamfir AD.

Biochimie. 2019 Aug;163:142-151. doi: 10.1016/j.biochi.2019.05.017. Epub 2019 Jun 13.

PMID:
31201844
2.

Abnormal level of CUL4B-mediated histone H2A ubiquitination causes disruptive HOX gene expression.

Lin Y, Yu J, Wu J, Wang S, Zhang T.

Epigenetics Chromatin. 2019 Apr 16;12(1):22. doi: 10.1186/s13072-019-0268-7.

3.

Anencephaly; the maternal experience of continuing with the pregnancy. Incompatible with life but not with love.

O'Connell O, Meaney S, O'Donoghue K.

Midwifery. 2019 Apr;71:12-18. doi: 10.1016/j.midw.2018.12.016. Epub 2018 Dec 25.

PMID:
30640134
4.

Best Mode of Delivery for Fetal Life-Limiting Conditions.

Cooper S, Williams NS.

Obstet Gynecol. 2019 Feb;133(2):368-371. doi: 10.1097/AOG.0000000000003065.

PMID:
30633136
5.

Mickey mouse signs.

Xiang H, Han J, Ridley WE, Ridley LJ.

J Med Imaging Radiat Oncol. 2018 Oct;62 Suppl 1:92. doi: 10.1111/1754-9485.39_12784. No abstract available.

PMID:
30309172
6.

A 2017 global update on folic acid-preventable spina bifida and anencephaly.

Kancherla V, Wagh K, Johnson Q, Oakley GP Jr.

Birth Defects Res. 2018 Aug 15;110(14):1139-1147. doi: 10.1002/bdr2.1366. Epub 2018 Aug 2.

PMID:
30070772
7.

Maternal association and influence of DHFR 19 bp deletion variant predisposes foetus to anencephaly susceptibility: a family-based triad study.

Prasoona KR, Sunitha T, Srinadh B, Muni Kumari T, Jyothy A.

Biomarkers. 2018 Nov;23(7):640-646. doi: 10.1080/1354750X.2018.1471619. Epub 2018 May 15.

PMID:
29708443
8.

Anencephaly and obstetric outcome beyond the age of viability.

Al-Obaidly S, Thomas J, Abu Jubara M, Al Ibrahim A, Al-Belushi M, Saleh N, Al-Mansouri Z, Khenyab N.

J Perinat Med. 2018 Oct 25;46(8):885-888. doi: 10.1515/jpm-2017-0363.

PMID:
29570453
9.

Countries with an immediate potential for primary prevention of spina bifida and anencephaly: Mandatory fortification of wheat flour with folic acid.

Kancherla V.

Birth Defects Res. 2018 Jul 3;110(11):956-965. doi: 10.1002/bdr2.1222. Epub 2018 Mar 13.

PMID:
29532629
10.

Genetic and functional analysis of SHROOM1-4 in a Chinese neural tube defect cohort.

Chen Z, Kuang L, Finnell RH, Wang H.

Hum Genet. 2018 Mar;137(3):195-202. doi: 10.1007/s00439-017-1864-x. Epub 2018 Feb 8.

11.

Prenatal diagnosis of sirenomelia with anencephaly and craniorachischisis totalis: A case report study.

Theofanakis C, Theodora M, Sindos M, Daskalakis G.

Medicine (Baltimore). 2017 Dec;96(50):e9020. doi: 10.1097/MD.0000000000009020.

12.

Malformations among infants of mothers with insulin-dependent diabetes: Is there a recognizable pattern of abnormalities?

Nasri HZ, Houde Ng K, Westgate MN, Hunt AT, Holmes LB.

Birth Defects Res. 2018 Jan;110(2):108-113. doi: 10.1002/bdr2.1155.

PMID:
29377640
13.

A targeted sequencing panel identifies rare damaging variants in multiple genes in the cranial neural tube defect, anencephaly.

Ishida M, Cullup T, Boustred C, James C, Docker J, English C; GOSgene, Lench N, Copp AJ, Moore GE, Greene NDE, Stanier P.

Clin Genet. 2018 Apr;93(4):870-879. doi: 10.1111/cge.13189. Epub 2018 Feb 11.

14.
15.

Molecular cytogenetic characterization of a duplication of 15q24.2-q26.2 associated with anencephaly and neural tube defect.

Chen CP, Chen CY, Chern SR, Wu PS, Chen SW, Lai ST, Lee CC, Yang CW, Wang W.

Taiwan J Obstet Gynecol. 2017 Aug;56(4):550-553. doi: 10.1016/j.tjog.2017.06.003.

16.

Neural tube closure and embryonic metabolism.

Yamaguchi Y, Miyazawa H, Miura M.

Congenit Anom (Kyoto). 2017 Sep;57(5):134-137. doi: 10.1111/cga.12219. Epub 2017 May 31. Review.

PMID:
28295633
17.

A detailed musculoskeletal study of a fetus with anencephaly and spina bifida (craniorachischisis), and comparison with other cases of human congenital malformations.

Alghamdi MA, Ziermann JM, Gregg L, Diogo R.

J Anat. 2017 Jun;230(6):842-858. doi: 10.1111/joa.12601. Epub 2017 Mar 7.

18.

A homozygous mutation in TRIM36 causes autosomal recessive anencephaly in an Indian family.

Singh N, Kumble Bhat V, Tiwari A, Kodaganur SG, Tontanahal SJ, Sarda A, Malini KV, Kumar A.

Hum Mol Genet. 2017 Mar 15;26(6):1104-1114. doi: 10.1093/hmg/ddx020.

PMID:
28087737
19.

Anomalies fœtales affectant le tube neural : Dépistage / diagnostic prénatal et prise en charge de la grossesse.

Wilson RD.

J Obstet Gynaecol Can. 2016 Dec;38(12S):S496-S511. doi: 10.1016/j.jogc.2016.09.059. Epub 2017 Jan 4. No abstract available.

PMID:
28063560
20.

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