Human Genome Epidemiology Literature Finder
Records 1 - 8 (of 8 Records) |
Query Trace: Abnormalities and MAX[original query] |
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The 5-HTTLPR polymorphism, platelet serotonin transporter activity and platelet serotonin content in underweight and weight-recovered females with anorexia nervosa. European archives of psychiatry and clinical neuroscience 2010 Sep 260 (6): 483-90. Ehrlich Stefan, Franke Leonora, Scherag Susann, Burghardt Roland, Schott Regina, Schneider Nora, Brockhaus Simone, Hein Jakob, Uebelhack Ralf, Lehmkuhl Ulri |
G-protein ß3 subunit 825CC genotype is associated with postprandial distress syndrome with impaired gastric emptying and with the feeling of hunger in Japanese. Neurogastroenterology and motility : the official journal of the European Gastrointestinal Motility Society 2011 Dec 23 (12): 1073-80. Shimpuku M, Futagami S, Kawagoe T, Nagoya H, Shindo T, Horie A, Kodaka Y, Itoh T, Sakamoto |
Testing new susceptibility genes in the cohort of apparently sporadic phaeochromocytoma/paraganglioma patients with clinical characteristics of hereditary syndromes. Clinical endocrinology 2013 Dec 79 (6): 817-23. P?czkowska Mariola, Kowalska Aldona, Sygut Jacek, Waligórski Dariusz, Malinoc Angelica, Janaszek-Sitkowska Hanna, Prejbisz Aleksander, Januszewicz Andrzej, Neumann Hartmut P |
Effect of creatine supplementation on physical performance are related to the AMPD1 and PPARG genes polymorphisms in football players. Rossi?skii fiziologicheski? zhurnal imeni I.M. Sechenova / Rossi?skaia akademiia nauk 2014 Jun 100 (6): 767-76. Lifanov D, Khadyeva M N, Rahmatullina L Sh, Demenev S V, Ibragimov R |
Prevalence of Cytogenetic Anomalies in Couples with Recurrent Miscarriages: A Case-control Study. Journal of human reproductive sciences 2018 2 10 (4): 302-309. Kalotra Vishali, Lall Meena, Saviour Pushpa, Verma Ishwar Chander, Kaur Anup |
Epilepsy in a cohort of children with Noonan syndrome and related disorders. European journal of pediatrics 2022 5 181 (8): 2919-2926. Davico Chiara, D'Alessandro Rossella, Borgogno Marta, Campagna Filippa, Torta Francesca, Ricci Federica, Amianto Federico, Vittorini Roberta, Carli Diana, Mussa Alessandro, Vitiello Benedetto, Ferrero Giovanni Battis |
Caveolin-1 rs1997623 variant and adult metabolic syndrome-Assessing the association in three ethnic cohorts of Arabs, South Asians and South East Asians. Frontiers in genetics 2022 11 13 1034892. Al Madhoun Ashraf, Hebbar Prashantha, Nizam Rasheeba, Haddad Dania, Melhem Motasem, Abu-Farha Mohamed, Thanaraj Thangavel Alphonse, Al-Mulla Fa |
Risk factors for coronary artery abnormalities and resistance to immunoglobulin plus ciclosporin A therapy in severe Kawasaki disease: subanalysis of the KAICA trial, randomized trial for cicrosporin A as the first-line treatment. Frontiers in pediatrics 2024 1 11 1321533. Yuri Murayama, Hiromichi Hamada, Yuki Shiko, Yoshihiro Onouchi, Nobuyuki Kakimoto, Yoshihito Ozawa, Hideki Hanaoka, Akira Hata, Hiroyuki Suzu |
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