HuGE Literature Finder
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| Maternal germline factors associated with aneuploid pregnancy loss: a systematic review. Human reproduction update 2021 . Blyth Ursula, Craciunas Laurentiu, Hudson Gavin, Choudhary Meenaks |
| Methylenetetrahydrofolate reductase gene polymorphisms are not associated with embryo chromosomal abnormalities and IVF outcomes. Systems biology in reproductive medicine 2021 May 1-11. Morales Ruth, Lledó Belén, Ortiz José A, Cascales Alba, Codina Helena, Rodríguez-Arnedo Adoración, Llácer Joaquin, Bernabeu Andrea, Bernabeu Rafa |
| May the morphological findings in the first-trimester abortion materials be indicative of inherited thrombophilia? The journal of obstetrics and gynaecology research 2020 Aug . Kaymaz Esin, Gun Banu D, Genc Gunes C, Kokturk Furuzan, Ozmen Kazim |
| The Correlation Between Abnormal Uterine Artery Flow in the First Trimester and Genetic Thrombophilic Alteration: A Prospective Case-Controlled Pilot Study. Diagnostics (Basel, Switzerland) 2020 Aug 10 (9): . Vedmedovska Natalija, Bokucava Diana, Kivite-Urtane Anda, Rovite Vita, Zake-Nikitina Liene, Klovins Janis, Fodina Violeta, Donders Gilbert G |
| Are Congenital Urinary Tract Abnormalities Linked to Maternal Methylenetetrahydrofolate Reductase Polymorphisms in Fetuses of Intentionally Terminated Pregnancies with Oligo- or Anhydramnios ? Fetal and pediatric pathology 2018 May 1-7. Beksac M Sinan, Beksac Alp Tuna, Buyukeren Melek, Tanacan Atakan, Bektas Hatice, Gucer Saf |
| Comparison of two groups for the apolipoprotein E polymorphisms by using next generation sequencing: The first group with three consecutive abortions and the second group with at most one abortion in three consecutive pregnancies. Gene 2018 May . Gumus Evr |
| Characteristics and Long-Term Prognosis of Patients =35 Years of Age with ST Segment Elevation Myocardial Infarction and "Normal or Near Normal" Coronary Arteries. The American journal of cardiology 2017 Jun . Rallidis Loukianos S, Gialeraki Argyri, Triantafyllis Andreas S, Tsirebolos Georgios, Liakos Georgios, Moutsatsou Paraskevi, Iliodromitis Efstathi |
| Associations of recurrent miscarriages with chromosomal abnormalities, thrombophilia allelic polymorphisms and/or consanguinity in Saudi Arabia. BMC medical genetics 2016 Oct 17 (Suppl 1): 69. Turki Rola F, Assidi Mourad, Banni Huda A, Zahed Hanan A, Karim Sajjad, Schulten Hans-Juergen, Abu-Elmagd Muhammad, Rouzi Abdulrahim A, Bajouh Osama, Jamal Hassan S, Al-Qahtani Mohammed H, Abuzenadah Adel |
| The efficacy of tissue factor -603A/G and +5466A>G polimorphisms at the development of venous thromboembolism in cancer patients. Experimental oncology 2016 Sep 38 (3): 187-90. Ero?lu A, Ceylan G G, Ozturk E, Yalcin A, Yalcin B, Karasoy |
| The incidence of severe intraventricular hemorrhage based on retrospective analysis of 35939 full-term newborns-report of two cases and review of literature. Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery 2016 Jul . Szpecht Dawid, Frydryszak Dagmara, Miszczyk Norbert, Szymankiewicz Marta, Gadzinowski Janu |
| Association between genetic polymorphisms in folate-related enzyme genes and infertile men with non-obstructive azoospermia. Systems biology in reproductive medicine 2015 Oct 61 (5): 286-92. Kim Shin Young, Lim Jung Wook, Kim Jin Woo, Park So Yeon, Seo Ju T |
| Variants in MTHFR gene and neural tube defects susceptibility in China. Metabolic brain disease 2015 Aug 30 (4): 1017-26. Wang Yongxin, Liu Yuan, Ji Wenyu, Qin Hu, Wu Hao, Xu Danshu, Turtuohut Tukebai, Wang Zenglia |
| A preliminary study of inherited thrombophilic risk factors in different clinical manifestations of venous thromboembolism in central Iran. The Indian journal of medical research 2015 Jul 142 (1): 46-52. Karimi Ali, Abolhasani Marziyeh, Hashemzadeh-Chaleshtori Morteza, Pourgheysari Bato |
| Association of Vitamin B12 Deficiency with Homozygosity of the TT MTHFR C677T Genotype, Hyperhomocysteinemia, and Endothelial Cell Dysfunction. The Israel Medical Association journal : IMAJ 2015 May 17 (5): 288-92. Shiran Avinoam, Remer Eric, Asmer Ihab, Karkabi Basheer, Zittan Eran, Cassel Aliza, Barak Mira, Rozenberg Orit, Karkabi Khaled, Flugelman Moshe |
| Cerebral ultrasound abnormalities in offsprings of women with C677T homozygous mutation in the MTHFR gene: a prospective study. World journal of pediatrics : WJP 2015 May 11 (2): 134-40. Pogliani Laura, Cerini Chiara, Penagini Francesca, Duca Piergiorgio, Mameli Chiara, Zuccotti Gian Vincen |
| Common Mutations of the Methylenetetrahydrofolate Reductase (MTHFR) Gene in Non-Syndromic Cleft Lips and Palates Children in North-West of Iran. Iranian journal of otorhinolaryngology 2015 Jan 27 (78): 7-14. Abdollahi-Fakhim Shahin, Asghari Estiar Mehrdad, Varghaei Parizad, Alizadeh Sharafi Mahdi, Sakhinia Masoud, Sakhinia Ebrah |
| Elevated risk of thrombophilia in agenesis of the vena cava as a factor for deep vein thrombosis. Orphanet journal of rare diseases 2015 10 (1): 3. Sagban Tolga Atilla, Scharf Rüdiger E, Wagenhäuser Markus U, Oberhuber Alexander, Schelzig Hubert, Grabitz Klaus, Duran Mans |
| Excess of rare variants in genes that are key epigenetic regulators of spermatogenesis in the patients with non-obstructive azoospermia. Scientific reports 2015 5 8785. Li Zesong, Huang Yi, Li Honggang, Hu Jingchu, Liu Xiao, Jiang Tao, Sun Guangqing, Tang Aifa, Sun Xiaojuan, Qian Weiping, Zeng Yong, Xie Jun, Zhao Wei, Xu Yu, He Tingting, Dong Chengliang, Liu Qunlong, Mou Lisha, Lu Jingxiao, Lin Zheguang, Wu Song, Gao Shengjie, Guo Guangwu, Feng Qiang, Li Yingrui, Zhang Xiuqing, Wang Jun, Yang Huanming, Wang Jian, Xiong Chengliang, Cai Zhiming, Gui Yaoti |
| Hyperhomocysteinemia and MTHFR polymorphisms as antenatal risk factors of white matter abnormalities in two cohorts of late preterm and full term newborns. Oxidative medicine and cellular longevity 2015 2015 543134. Marseglia Lucia M, Nicotera Antonio, Salpietro Vincenzo, Giaimo Elisa, Cardile Giovanna, Bonsignore Maria, Alibrandi Angela, Caccamo Daniela, Manti Sara, D'Angelo Gabriella, Mamì Carmelo, Di Rosa Gabriel |
| Epistasis between polymorphisms in COMT, ESR1, and GCH1 influences COMT enzyme activity and pain. Pain 2014 Nov 155 (11): 2390-9. Smith Shad B, Reenilä Ilkka, Männistö Pekka T, Slade Gary D, Maixner William, Diatchenko Luda, Nackley Andrea |
| Profile of prothrombotic factors in Indian children with ischemic stroke. Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia 2014 Aug 21 (8): 1315-8. Konanki Ramesh, Gulati Sheffali, Saxena Renu, Gupta Arun Kumar, Seith Ashu, Kumar Ashok, Saxena Anita, Kabra Madhulika, Kalra Veena, Lakshmy Ramakrishn |
| Methylenetetrahydrofolate reductase gene variants and antipsychotic-induced weight gain and metabolic disturbances. Journal of psychiatric research 2014 Jul 54 36-42. Kao A C C, Rojnic Kuzman M, Tiwari A K, Zivkovic M V, Chowdhury N I, Medved V, Kekin I, Zai C C, Lieberman J A, Meltzer H Y, Bozina T, Bozina N, Kennedy J L, Sertic J, Müller D |
| Analysis of MTHFR Gene C.677C>T and C.1298A>C Polymorphisms in Iranian Patients with Non-Syndromic Cleft Lip and Palate. Iranian journal of public health 2014 Jun 43 (6): 821-7. Jahanbin Arezoo, Hasanzadeh Nadia, Abdolhoseinpour Faraneh, Sadr-Nabavi Ariane, Raisolsadat Mohammad-Ali, Shamsian Khosro, Mohajertehran Farnaz, Kianifar Hamidre |
| [Methylenetetrahydrofolate reductase polymorphisms as risk factors for myelomeningocele]. Revista médica de Chile 2014 May 142 (5): 587-92. Pardo Rosa, Suazo José, Castillo Silvia, Vargas Marcela, Zalavari Andrea, Santos José Luis, Blanco Rafael, Rotter Karin, Solar Margarita, Tapia E |
| Association of ADRA2A and MTHFR gene polymorphisms with weight loss following antipsychotic switching to aripiprazole or ziprasidone. Human psychopharmacology 2014 Jan 29 (1): 38-45. Roffeei Siti Norsyuhada, Reynolds Gavin P, Zainal Nor Zuraida, Said Mas Ayu, Hatim Ahmad, Aida Syarinaz Ahmad, Mohamed Zahur |
| Association of neural tube defects in children of mothers with MTHFR 677TT genotype and abnormal carbohydrate metabolism risk: a case-control study. Genetics and molecular research : GMR 2014 13 (1): 2200-7. Cadenas-Benitez N M, Yanes-Sosa F, Gonzalez-Meneses A, Cerrillos L, Acosta D, Praena-Fernandez J M, Neth O, Gomez de Terreros I, Ybot-González |
| Methylenetetrahydrofolate reductase gene A1298C polymorphism and susceptibility to recurrent pregnancy loss: a meta-analysis. Cellular and molecular biology (Noisy-le-Grand, France) 2014 60 (2): 27-34. Rai |
| Etiological risk factors for subfertility among Palestinian women in Gaza. Journal of biomedical research 2013 Mar 27 (2): 127-34. Sirdah Mahmoud Mohammed, Abushahla Abdelnasser Kassem, Ghalayeni Bahaa Yousif, Aburamadan Ahmed Gam |
| [Evaluation of coagulopathies and fibrinolytic abnormalities in central retinal vein occlusion in patients under 60 years of age]. Journal francais d'ophtalmologie 2012 Dec . Tea S, Barrali M, Racadot E, Delbosc B |
| Bladder exstrophy-epispadias complex and the role of methylenetetrahydrofolate reductase C677T polymorphism: A case control study. Journal of Indian Association of Pediatric Surgeons 0 21 (1): 28-32. Raman Venkat Shankar, Bajpai Minu, Ali Ab |
- Page last reviewed:Oct 1, 2021
- Page last updated:Dec 01, 2021
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