Results 271 to 280 of about 777,565 (394)

KIDINS220 Variant Associated With Hypoplasia of the Corpus Callosum and Aqueduct Stenosis

Prenatal Diagnosis, EarlyView.
ABSTRACT KIDINS220 plays a key role in neuronal survival, differentiation, and synaptic function. Abnormalities in its expression have been linked postnatally to neurodevelopmental disorders and SINO syndrome though prenatal presentations are rarely described.
Kimia Ghannad‐Zadeh, Patrick Shannon, Rebekah Jobling, Elka Miller, Karen Chong, Erin Mathews, David Chitayat, Shiri Shinar   +7 more
wiley   +1 more source

Low-molecular-weight heparin in the prevention of unexplained recurrent miscarriage: a systematic review and meta-analysis. [PDF]

Sci Rep
Scarrone M, Salmeri N, Buzzaccarini G, Canti V, Pasi F, Papaleo E, Rovere-Querini P, Candiani M, Alteri A, Busnelli A, Vanni VS.   +10 more
europepmc   +1 more source

A homozygous KASH5 frameshift mutation causes diminished ovarian reserve, recurrent miscarriage, and non-obstructive azoospermia in humans. [PDF]

Front Endocrinol (Lausanne), 2023
Hou X, Zeb A, Dil S, Zhou J, Zhang H, Shi B, Muhammad Z, Khan I, Zaman Q, Shah WA, Jiang X, Wu L, Ma H, Shi Q.   +13 more
europepmc   +1 more source

Prevention of recurrent miscarriage for women with antiphospholipid antibody or lupus anticoagulant [PDF]

, 2005
Marianne Empson, Marissa Lassere, Jonathan C. Craig, James R. Scott   +3 more
openalex   +1 more source

Characteristic Analysis of Ultrasound Diagnosis of Limb Body Wall Complex in Early Pregnancy

Prenatal Diagnosis, EarlyView.
ABSTRACT This study aims to explore the diagnostic value of prenatal ultrasound in limb body wall complex (LBWC) during pregnancy and to improve the understanding of LBWC for early ultrasound diagnosis. The ultrasound data and follow‐up results of 107 cases of LBWC (predominantly diagnosed in the first trimester) from the Third Affiliated Hospital of ...
Lingling Zhang, Rui Wang, Yueshu Zhao, Juan Wu, Hezhou Li, Mengna Li   +5 more
wiley   +1 more source

Comparison of the gene expression profiles of endometrial and trophoblastic cells in women with recurrent miscarriage: A bioinformatics approach. [PDF]

Int J Reprod Biomed
Ahmadi K, Reiisi S, Habibi Z.
europepmc   +1 more source

Mutation of FLNA attenuating the migration of abdominal muscles contributed to Melnick-Needles syndrome (MNS) in a family with recurrent miscarriage. [PDF]

Mol Genet Genomic Med, 2023
Luo X, Yang Z, Zeng J, Chen J, Chen N, Jiang X, Wei Q, Yi P, Xu J.   +8 more
europepmc   +1 more source

Altered expression of genes involved in the production and degradation of endometrial extracellular matrix in patients with unexplained infertility and recurrent miscarriages

, 2002
Varpu Jokimaa, Sanna Oksjoki, Harry Kujari, Eero Vuorio, Leena Anttila   +4 more
openalex   +1 more source

Recurrent miscarriage and long-term thrombosis risk: a case–control study [PDF]

, 2005
Siobhan Quenby, Roy G. Farquharson, F. Dawood, Ann M. Hughes, J. Topping   +4 more
openalex   +1 more source

Clinical Laboratory Experience With Prenatal cfDNA Screening in Triplet Pregnancies

Prenatal Diagnosis, EarlyView.
ABSTRACT Objective Prenatal cfDNA screening is the most sensitive and specific screen for common aneuploidies in singleton and twin pregnancies and has been endorsed by several professional societies as a first‐tier screen or contingent screen. However, data for triplet pregnancies is lacking, as these pregnancies are relatively uncommon and obtaining ...
Erica Soster, Brittany Dyr, Samantha Caldwell, Savannah Moore, Eyad Almasri, Hany Magharyous, Juan‐Sebastian Saldivar, Phillip Cacheris   +7 more
wiley   +1 more source