Results 71 to 80 of about 926,075 (161)

Identification of Risk‐Related Prenatal Medication Exposure Profiles for Childhood Asthma Using the Bayesian Profile Regression: A Cohort Study Using the POMME Cohort

Pharmacoepidemiology and Drug Safety, Volume 35, Issue 11, November 2026.
ABSTRACT Purpose To identify prenatal medication exposure profiles associated with childhood asthma. Methods This population‐based cohort study used data from the POMME (PrescriptiOn Médicaments Mères Enfants) cohort, including 18 851 children born in the Haute‐Garonne area (France) in 2010 and 2015, and followed until 2023.
Solène Russo, Justine Bénévent, Anna‐Belle Beau   +2 more
wiley   +1 more source

Permanent Congenital Hypothyroidism in Very Low Birth Weight Infants: A Single Center’s Experience [PDF]

Neonatal Medicine
Purpose Congenital hypothyroidism (CH) is a major preventable cause of intellectual disability, particularly in very low birth weight (VLBW) infants, who are at increased risk due to hypothalamic-pituitary-thyroid axis immaturity.
Joo Hyung Roh, Tae-Gyeong Kim, Keon Hee Seol, Chae Young Kim, Soo Hyun Kim, Ji Yoon Jeong, Ja Hye Kim, Euiseok Jung, Jin-Ho Choi, Byong Sop Lee   +9 more
doaj   +1 more source

Integrated Reproductive and Cytogenetic Assessment of Infertility in a Captive Jaguar (Panthera onca)

Veterinary Medicine and Science, Volume 12, Issue 6, November 2026.
Integrated reproductive and cytogenetic assessment of infertility in a captive jaguar pair identified normal chromosomal status in both individuals, whereas impaired semen quality in the male likely represents a major limiting factor for reproductive success under the observed conditions.
Marie Altmanová, Julie Strand, Kathrine Thejll Kirchhoff, Zuzana Majtánová   +3 more
wiley   +1 more source

Permanent and transient congenital hypothyroidism in full-term and preterm born infants [PDF]

Thyroid Research, 2013
Congenital hypothyroidism (CH) is one of the most common endocrine disorders in the infant population. It is also one of the most important causes of foreseeable brain damage and severe mental impairment. Current views on CH pathogenesis, screening schema and treatment standards have been presented.
Petriczko, Elżbieta, Walczak, Mieczysław   +1 more
openaire   +1 more source

The Lupus Damage Index Revision Program: Results From the Item Generation and Reduction Phases

Arthritis Care &Research, Volume 78, Issue 10, Page 1449-1466, October 2026.
Objective A data‐driven and expert/patient consensus‐based project to develop a revised Systemic Lupus International Collaborating Clinics (SLICC)/American College of Rheumatology (ACR) Damage Index (SDI) is under way supported by SLICC, ACR, and the Lupus Foundation of America. Our objective is to report the item generation and reduction phase results
Burak Kundakci, Megan R. W. Barber, Ann E. Clarke, Sindhu R. Johnson, Anselm Mak, Hermine I. Brunner, Murat Inanc, Rosalind Ramsey‐Goldman, Guillermo Ruiz‐Irastorza, Ellen M. Ginzler, John G. Hanly, Alexandra Legge, Cynthia Aranow, Laurent Arnaud, Nathalie Costedoat‐Chalumeau, Dafna D. Gladman, Søren Jacobsen, Michelle Petri, Clovis A. Silva, Évelyne Vinet, Alexandre E. Voskuyl, SDI Revision Literature Review Groups, SDI Revision Delphi Panel, SDI Revision Item Reduction Committee, SDI Revision Clinical Domain Groups, Ian N. Bruce   +25 more
wiley   +1 more source

De Novo 2.2 Mb 19q13.42–q13.43 Microdeletion Encompassing U2AF2: Support for a Haploinsufficiency Model

American Journal of Medical Genetics Part A, Volume 200, Issue 10, Page 2350-2356, October 2026.
ABSTRACT U2 small nuclear RNA auxiliary factor 2 (U2AF2) is an essential pre‐mRNA splicing factor involved in the early stages of pre‐mRNA splicing. To date, multiple individuals have been reported with predominantly heterozygous missense variants presenting intellectual disability, speech and motor delays, seizures, hypotonia, and thin or hypoplastic ...
Amanda Toledo, Sarah Araji, Weimin Bi, Seema R. Lalani   +3 more
wiley   +1 more source

Epidemiological of the Different Forms of Permanent Primary Congenital Hypothyroidism and Associated Malformations [PDF]

Pediatric Research, 1999
Epidemiological of the Different Forms of Permanent Primary Congenital Hypothyroidism and Associated ...
Heidi Devos, Celia Rodd, Nancy Gagne, Rachel Laframboise, Guy Van Vliet   +4 more
openaire   +1 more source

Case‐malformed signal detection and prioritisation using EUROmediCAT data for pharmacovigilance in pregnancy

British Journal of Clinical Pharmacology, Volume 92, Issue 10, Page 3586-3597, October 2026.
Aim Many women take medications during pregnancy. However, the risk to the fetus from most medications is uncertain. Congenital anomalies are one of the leading causes of infant death and contribute to long‐term disability. Signal detection methods can be used to systematically identify possible medication–anomaly associations that require further ...
Hannah Johnson, Helen Dolk, Maria Loane, Christine Damase‐Michel, Joanne Given, Hedvig Nordeng, Jorieke E. H. Bergman, Iain Carey, Elly Den Hond, Ester Garne, Florence Rouget, Lea Bruneau, Isabelle Monier, Anke Rissmann, Mary O'Mahony, Miriam Gatt, Renée Lutke, Joanna Sichitiu, Elisa Ballardini, Alessio Coi, Clara Cavero Carbonell, David Tucker, Joan Morris   +22 more
wiley   +1 more source

Congenital hypothyroidism with goiter

, 2011
The article provides a description of congenital hypothyroidism and goiter in a newborn ...

core   +1 more source

Congenital Hypothyroidism: Etiology and Growth-Development Outcome

Acta Medica Iranica, 2014
One of the most preventable causes of mental and growth retardation is congenital hypothyroidism (CH). This study tries to investigate growth and mental outcome of patients with CH. Since November 2006 and November 2007 in Guilan province, north of Iran,
Setila Dalili, Seyed Mahmood Rezvani, Hossein Dalili, Zahra Mohtasham Amiri, Hamid Mohammadi, Sahar Abrisham Kesh, Mohammad Hassan Novin, Abdolreza Medghalchi, Hajar Gholamnezhad   +8 more
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