IVF

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IVF

abbr.
in vitro fertilization
American Heritage® Dictionary of the English Language, Fifth Edition. Copyright © 2016 by Houghton Mifflin Harcourt Publishing Company. Published by Houghton Mifflin Harcourt Publishing Company. All rights reserved.

IVF

abbreviation for
(Medicine) in vitro fertilization
Collins English Dictionary – Complete and Unabridged, 12th Edition 2014 © HarperCollins Publishers 1991, 1994, 1998, 2000, 2003, 2006, 2007, 2009, 2011, 2014

IVF

in vitro fertilization.
Random House Kernerman Webster's College Dictionary, © 2010 K Dictionaries Ltd. Copyright 2005, 1997, 1991 by Random House, Inc. All rights reserved.
Translations

IVF

N ABBR =in vitro fertilization → FIV f
Collins Spanish Dictionary - Complete and Unabridged 8th Edition 2005 © William Collins Sons & Co. Ltd. 1971, 1988 © HarperCollins Publishers 1992, 1993, 1996, 1997, 2000, 2003, 2005

IVF

[ˌaɪviːˈɛf] n (=in vitro fertilization) → FIV f(= fécondation in vitro)
Collins English/French Electronic Resource. © HarperCollins Publishers 2005

IVF

abbr in vitro fertilization. V. fertilization.
English-Spanish/Spanish-English Medical Dictionary Copyright © 2006 by The McGraw-Hill Companies, Inc. All rights reserved.
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References in periodicals archive ?
Postmortem molecular analysis of KCNQ1 and SCN5A genes in sudden unexplained death in young Australians.
Consideration of molecular autopsies in forensic cases of sudden unexpected death in infants and children in South Africa
Major ion channels, like SCN5A, L-type [Ca.sup.2+] channel, [I.sub.to], [I.sub.Kr], [I.sub.Ks], and [I.sub.K1], play critical roles in the electrical activities and functions of healthy and diseased cardiomyocytes.
Ion Channel Expression and Characterization in Human Induced Pluripotent Stem Cell-Derived Cardiomyocytes
The primary mechanism of BrS is mutations in the SCN5A gene, which are responsible for regulation of the alpha subunit of sodium channels in the cell membrane of cardiac muscle (3).
A Report of Brugada Syndrome Presenting with Cardiac Arrest Triggered by Verapamil Intoxication
(13) Multiple predictors of future arrhythmic events in patients with the Brugada pattern were studied, with male gender, mutation of the SCN5A gene and a positive family history of SCD found to be non -predictive.
Fever-induced Brugada pattern misdiagnosed as an acute myocardial infarction
Genetic testing was positive for a heterozygous mutation in the sodium voltage-gated channel alpha subunit 5 (SCN5A) gene with a p.
A variant of Brugada syndrome
Variants in 3 ion channel genes account for over 70% of patients with a definitive diagnosis of LQTS (13, 14) [although the yield is substantially less for all referral cases (15)]: loss of function variants in the potassium ion channel genes potassium voltage-gated channel subfamily Q member 1 (KCNQ1) and potassium voltage-gated channel subfamily H member 2 (KCNH2; LQT1 and LQT2 respectively) and gain of function variants in the sodium ion channel gene sodium voltage-gated channel alpha a subunit 5 (SCN5A; LQT3).
Issues and Challenges in Diagnostic Sequencing for Inherited Cardiac Conditions
Deng et al., "Whole-exome sequencing identifies Y1495X of SCN5A to be associated with familial conduction disease and sudden death," Scientific Reports, vol.
Detection of Folliculin Gene Mutations in Two Chinese Families with Birt-Hogg-Dube Syndrome
A SCN5A gene variant (R1193Q) was identified after birth, which might have attributed to the complex arrhythmias in this patient.
Prenatal Diagnosis of Atrioventricular Block and QT Interval Prolongation by Fetal Magnetocardiography in a Fetus with Trisomy 18 and SCN5A R1193Q Variant
At first it was thought Fiona, of Annitsford, may had suffered Sudden Arrhythmia Death Syndrome (SADS) but tests later showed she was suffering from a faulty gene called SCN5A. This mutation was the probable cause of her death.
Tragic mum will live on through daughter Olivia; TRIBUTES PLANNED AFTER NORTH EAST WOMAN DIES SUDDENLY AGED JUST 24
Although iPSC-CMs express relevant ion channel genes (SCN5A, KCNJ2, CACNA1C, KCNQ1, and KCNH2), structural genes (MYH6, MYLPF, MYBPC3, DES, TNNT2, and TNNI3), and transcription factors (NKX2.5, GATA4, and GATA6) [77], they differ from adult ventricular cardiomyocytes in a number of properties.
Human induced pluripotent stem cell-derived cardiomyocytes afford new opportunities in inherited cardiovascular disease modeling
Gene mutations in KCNQ1, KCNH2 and SCN5A account for 90% to 95% cases of long QT syndrome.
LONG SURVIVAL OF PATIENT WITH ROMANO WARD SYNDROME ON BETA BLOCKERS
[1] The pathology is due to gene mutation SCN5A located on 3p, [5] which codes for sodium ion channel on cell membranes of myocytes of heart.
Sudden cardiac arrest during general anaesthesia in an undiagnosed Brugada syndrome

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