Results 231 to 240 of about 105,581 (338)

Epidemiology of hypospadias in China: A nationwide surveillance‐based study, 2010–2020

Andrology, Volume 14, Issue 3, Page 880-889, March 2026.
Abstract Background The prevalence of hypospadias varied internationally. However, epidemiological data on hypospadias in contemporary China remain limited. Objectives We aim to examine the epidemiological characteristics of hypospadias in Chinese population.
Chen Zhiyu, Gao Yuyang, Xu Wenli, Li Wenyan, Liu Zhen, Zhou Jiayuan, Zhu Jun, Dai Li   +7 more
wiley   +1 more source

Synaptic and intrinsic membrane defects disrupt early neural network dynamics in Down syndrome. [PDF]

Nat Commun
Hannan SB, Alić I, Murray A, Kwon J, Mortensen M, Kang HJ, Plećaš A, Goh PA, O'Brien NL, Naud R, Nižetić D, Smart TG.   +11 more
europepmc   +1 more source

Anthropometric charts for infants with trisomies 21, 18, or 13 born between 22 weeks gestation and term: The VON charts

, 2012
Nansi S. Boghossian, Jeffrey D. Horbar, Jeffrey C. Murray, Joseph H. Carpenter, for the Vermont Oxford Network   +4 more
openalex   +2 more sources

The sensory penis: A comprehensive immunohistological and ontogenetic exploration of human penile innervation

Andrology, Volume 14, Issue 3, Page 661-701, March 2026.
Abstract Background Penile sexual sensation relies on intricate neural structures that remain incompletely characterized. Immunohistological insights into their development and organization can enhance understanding of penile neuroanatomy and function, while optimizing surgical outcomes.
Alfonso Cepeda‐Emiliani, María Otero‐Alén, Juan Suárez‐Quintanilla, Marina Gándara‐Cortés, Tomás García‐Caballero, Rosalía Gallego, Lucía García‐Caballero   +6 more
wiley   +1 more source

An Innovative Transitional Care Unit for Hospital to Home Transition of Children With Medical Complexity: A Qualitative Study of Parents' Experiences

Child: Care, Health and Development, Volume 52, Issue 2, March 2026.
ABSTRACT Background Hospital‐to‐home (H2H) transitions of children with medical complexity (CMC) are a multifaceted process with many challenges and obstacles, especially for parents. The ‘Jeroen Pit Huis’ (JPH) is a stand‐alone, innovative transitional care unit (TCU) that aims to improve the transition home.
Heleen N. Haspels, Nicole Skomorowski, Koen F. M. Joosten, Matthijs de Hoog, Job B. M. van Woensel, Clara D. van Karnebeek, Mattijs W. Alsem   +6 more
wiley   +1 more source

Beyond the Diagnosis: A Journey of an 8-Year-Old Girl with Patau Syndrome: Case Report. [PDF]

Children (Basel)
Aleksander N, Bukała A, Borowska W, Czapla K, Bylok K, Magiera M, Czerwiec T, Stencel-Gabriel K.   +7 more
europepmc   +1 more source

Prenatal Diagnosis of MSL2‐Related Ventriculomegaly in Association With an Inherited 15q13 Microduplication

Clinical Genetics, Volume 109, Issue 3, Page 581-585, March 2026.
We hereby report the first prenatal diagnosis of MSL2‐related pathology, namely ventriculomegaly. Favorable 11‐month follow‐up illustrates the challenges in predicting postnatal outcomes for genetic anomalies linked to recently characterized phenotypes with limited documented cases.
Omar Zgheib, Thomas Rio Frio, Jean‐Marie Pellegrinelli, Stefania Gimelli, Caterina Marconi, Delphine Le Mercier, Monica Rebollo Polo, Céline Habre, Joël Fluss, Russia Ha‐Vinh Leuchter, Marc Abramowicz, Rosalinda Giannini, Siv Fokstuen   +12 more
wiley   +1 more source

Prevalence of os odontoideum: a systematic review, meta-analysis and meta-regression with implications for vertebral artery and osseous anomalies. [PDF]

Neurosurg Rev
Klepinowski T, Osiowski A, Grzyb W, Esposito G, Osiowski M, Klepinowska M, Taterra D, Sagan L.   +7 more
europepmc   +1 more source

High Concordance of Copy Number Variants Detected by Chromosomal Microarray and Exome Sequencing in Clinical Diagnostics

Clinical Genetics, Volume 109, Issue 3, Page 529-538, March 2026.
To assess the relevance of exome sequencing as a first‐tier diagnostic tool, three aspects were investigated: detection of copy number variants (CNVs) from exomes as compared to chromosomal microarray, clinically‐relevant CNVs across all sizes, and additional diagnostic utilities (uniparental disomy and triploidy).
Rivka Birnbaum, Maya Slovik, Shamir Zenvirt, Ilana Livyatan, Israel Altman, Shiri Gershon, Jonathan Rips, Hagit Daum, Chaggai Rosenbluh, Orly Elpeleg, Vardiella Meiner, Ayala Frumkin, Hagar Mor‐Shaked, Tamar Harel   +13 more
wiley   +1 more source