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Matteo Cassina

Showing results (61-70 of 70) with videos related to

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American Journal of Human Genetics|May 29, 2018
Recessive Spondylocarpotarsal Synostosis Syndrome Due to Compound Heterozygosity for Variants in MYH3Sophia R Cameron-Christie, Constance F Wells, Marleen Simon, et al.
British Journal of Clinical Pharmacology|December 8, 2017
Pregnancy outcomes in women on metformin for diabetes or other indications among those seeking teratology information servicesAlice Panchaud, Valentin Rousson, Thierry Vial, et al.
Orphanet Journal of Rare Diseases|April 27, 2020
Telemedicine strategy of the European Reference Network ITHACA for the diagnosis and management of patients with rare developmental disordersMichael Smith, Elizabeth Alexander, Ruta Marcinkute, et al.
Acta Psychiatrica Scandinavica|December 18, 2023
Effects of maternal modafinil treatment on fetal development and neonatal growth parameters - a multicenter case series of the European Network of Teratology Information Services (ENTIS)Marlies Onken, Lukas Lohse, Bénédicte Coulm, et al.
Human Mutation|July 24, 2013
Recurrent HERV-H-mediated 3q13.2-q13.31 deletions cause a syndrome of hypotonia and motor, language, and cognitive delaysAndrey Shuvarikov, Ian M Campbell, Piotr Dittwald, et al.
Pediatric Neurology|February 11, 2023
Extended Glasgow Outcome Scale to Evaluate the Functional Impairment of Patients With Subcortical Band Heterotopia: A Multicentric Cross-sectional StudyIrene Toldo, Francesco Brunello, Paola Cavasin, et al.
Breast (Edinburgh, Scotland)|November 11, 2025
Subtype distribution, clinical presentation, and molecular spectrum of neurofibromatosis type 1-associated breast cancerNiccolò Di Giosaffatte, Paola Daniele, Francesco Petrizzelli, et al.
Medrxiv : the Preprint Server for Health Sciences|May 19, 2025
Genome-wide association studies of binge eating behaviour and anorexia nervosa yield insights into the unique and shared biology of eating disorder phenotypesJet D Termorshuizen, Helena L Davies, Sang-Hyuck Lee, et al.
Nature Genetics|July 17, 2019
Genome-wide association study identifies eight risk loci and implicates metabo-psychiatric origins for anorexia nervosaHunna J Watson, Zeynep Yilmaz, Laura M Thornton, et al.
Addiction Biology|February 18, 2020
Shared genetic risk between eating disorder- and substance-use-related phenotypes: Evidence from genome-wide association studiesMelissa A Munn-Chernoff, Emma C Johnson, Yi-Ling Chou, et al.
Pageof 7

Showing results (61-70 of 70) with videos related to

Sort By:
Pageof 7
You have reached the last page of results.This site can display upto 70 results.
American Journal of Human Genetics|May 29, 2018
Recessive Spondylocarpotarsal Synostosis Syndrome Due to Compound Heterozygosity for Variants in MYH3Sophia R Cameron-Christie, Constance F Wells, Marleen Simon, et al.
British Journal of Clinical Pharmacology|December 8, 2017
Pregnancy outcomes in women on metformin for diabetes or other indications among those seeking teratology information servicesAlice Panchaud, Valentin Rousson, Thierry Vial, et al.
Orphanet Journal of Rare Diseases|April 27, 2020
Telemedicine strategy of the European Reference Network ITHACA for the diagnosis and management of patients with rare developmental disordersMichael Smith, Elizabeth Alexander, Ruta Marcinkute, et al.
Acta Psychiatrica Scandinavica|December 18, 2023
Effects of maternal modafinil treatment on fetal development and neonatal growth parameters - a multicenter case series of the European Network of Teratology Information Services (ENTIS)Marlies Onken, Lukas Lohse, Bénédicte Coulm, et al.
Human Mutation|July 24, 2013
Recurrent HERV-H-mediated 3q13.2-q13.31 deletions cause a syndrome of hypotonia and motor, language, and cognitive delaysAndrey Shuvarikov, Ian M Campbell, Piotr Dittwald, et al.
Pediatric Neurology|February 11, 2023
Extended Glasgow Outcome Scale to Evaluate the Functional Impairment of Patients With Subcortical Band Heterotopia: A Multicentric Cross-sectional StudyIrene Toldo, Francesco Brunello, Paola Cavasin, et al.
Breast (Edinburgh, Scotland)|November 11, 2025
Subtype distribution, clinical presentation, and molecular spectrum of neurofibromatosis type 1-associated breast cancerNiccolò Di Giosaffatte, Paola Daniele, Francesco Petrizzelli, et al.
Medrxiv : the Preprint Server for Health Sciences|May 19, 2025
Genome-wide association studies of binge eating behaviour and anorexia nervosa yield insights into the unique and shared biology of eating disorder phenotypesJet D Termorshuizen, Helena L Davies, Sang-Hyuck Lee, et al.
Nature Genetics|July 17, 2019
Genome-wide association study identifies eight risk loci and implicates metabo-psychiatric origins for anorexia nervosaHunna J Watson, Zeynep Yilmaz, Laura M Thornton, et al.
Addiction Biology|February 18, 2020
Shared genetic risk between eating disorder- and substance-use-related phenotypes: Evidence from genome-wide association studiesMelissa A Munn-Chernoff, Emma C Johnson, Yi-Ling Chou, et al.
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