Results 301 to 310 of about 737,277 (397)

Eliminating left ventricular outlet stenosis lowers the risk for endocardial fibroelastosis recurrence†. [PDF]

Eur J Cardiothorac Surg
Gierlinger G, Diaz-Gil D, Tulzer A, Mair R, Sames-Dolzer E, Saraci K, Staffa SJ, Zurakowski D, Kreuzer M, Seeber F, Emani SM, Del Nido PJ, Mair R, Friehs I.   +13 more
europepmc   +1 more source

Papilloma of the Right Laryngeal Ventricle, with Blood Cyst of Vocal Cord

, 1922
James Atkinson
openalex   +1 more source

Genotype–Phenotype Correlation in TTC7A‐Associated Gastrointestinal Defects and Immunodeficiency Syndrome 1

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Gastrointestinal defects and immunodeficiency syndrome 1 (GIDID1) is a rare autosomal recessive disorder caused by biallelic variants in TTC7A. GIDID1 is characterized by a broad clinical spectrum ranging from very early‐onset inflammatory bowel disease (VEOIBD) to multiple intestinal atresia (MIA) with or without immunological manifestations.
Julia Imhoff, Hans Christian Schmidt, Matthias Hans Belau, Johanna Hagens, Mario Lange, Daniel Tegtmeyer, Konrad Reinshagen, Frederike Leonie Harms, Christian Tomuschat   +8 more
wiley   +1 more source

Global longitudinal strain as a predictor of outcomes in chronic Chagas´ cardiomyopathy. [PDF]

PLoS Negl Trop Dis
Romano MMD, Moreira HT, Alenezi F, Kisslo J, Lombo Lievano B, Schmidt A, Maciel BC, Marin-Neto JA, Velazquez EJ.   +8 more
europepmc   +1 more source

Poland Anomaly and Atretic Cephalocele in the Same Child: Coincidence or Association?

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Poland Anomaly is a rare congenital disorder typically characterized by hypoplasia or agenesis of pectoral muscle with or without ipsilateral limb hypoplasia. The association of central nervous system malformation with Poland Anomaly has been rarely reported and includes craniofacial dysplasia, microcephaly, and Dandy‐Walker malformation ...
Alessandra Greta Grassi, Silvia Pontesilli, Laura Demelas, Francesca Vigliani, Massimo Agosti, Angelo Selicorni   +5 more
wiley   +1 more source

Reliability of comprehensive echocardiography evaluation of patent ductus arteriosus among extremely preterm neonates across a national network: A prospective observational study. [PDF]

J Neonatal Perinatal Med
Weisz DE, Thomas L, Ye XY, Mertens L, Lapointe A, Villeneuve A, Altit G, Lalitha R, Ben Fadel N, Jacob G, Louis D, Bhattacharya S, Soraisham A, Hébert A, Mitra S, Hyderi A, Ting JY, Castaldo M, Surak A, Deshpande P, Elsayed Y, Jasani B, Nissimov S, Zhu F, Shah P, Jain A.   +25 more
europepmc   +1 more source

Trisomy 5p: Long Recognized, Rarely Published‐ Three New Cases and Review of the Literature

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Complete trisomy 5p is a rare chromosomal disorder caused by a duplication of the short arm of chromosome 5. Current data suggest that complete trisomy 5p presents as a distinct clinical syndrome including but not limited to seizures, developmental delays, facial dysmorphisms, failure to thrive, and recurrent respiratory infections.
Gabriela J. Kim, Kristen N. Lee, Amanda B. Pritchard   +2 more
wiley   +1 more source

An Atypical Left Ventricular Pseudoaneurysm Managed Conservatively. [PDF]

JACC Case Rep
Chong T, Babu A, Rajwani A, Best M.
europepmc   +1 more source

Intestinal Atresia in PPP1R12A‐Related Urogenital and Brain Malformation Syndrome

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT PPP1R12A‐related urogenital and brain malformation syndrome (UBMS) is a newly described disorder characterized by congenital anomalies primarily involving the urogenital system and the brain. We describe a preterm female neonate with multiple congenital anomalies, including type IIIb jejunal atresia, incomplete intestinal rotation, imperforate
Adriana Gomes, Sanjana Karamcheti, Álvaro Martín Rodriguez, Anna‐Kaisa Niemi, Lynne M. Bird   +4 more
wiley   +1 more source

Volumetric predictors for shunt-dependency in pediatric posterior fossa tumors. [PDF]

Sci Rep
Wilhelmy F, Güresir E, Wach J, Vychopen M, Nestler U, Prasse G, Haddad L, Kasper J, Wende T.   +8 more
europepmc   +1 more source