Results 201 to 210 of about 794,627 (318)

Intestinal Ultrasound-Assisted Endoscopic Management of Acute Bowel Obstruction in a Patient With Crohn's Disease. [PDF]

ACG Case Rep J
Miyatani Y, Choi NK, Krugliak Cleveland N, Rubin DT.   +3 more
europepmc   +1 more source

MicroRNA-29 in Aortic Dilation: Implications for Aneurysm Formation

Circulation Research, 2011
R. Boon, T. Seeger, S. Heydt, A. Fischer, Eduard Hergenreider, A. Horrevoets, M. Vinciguerra, N. Rosenthal, S. Sciacca, M. Pilato, Paula M. van Heijningen, J. Essers, R. Brandes, A. Zeiher, S. Dimmeler   +14 more
semanticscholar   +1 more source

The Novel ACTC1 p.Gly50Ser Variant Is Associated With Arrhythmia and Secondary Features of HCM Without Hypertrophy

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT The key diagnostic criterion for hypertrophic cardiomyopathy is the presence of otherwise unexplained hypertrophy. Current definitions of HCM rely on specific thresholds to establish a diagnosis, while guideline directed risk stratification algorithms take its magnitude into consideration.
Thomas D. Gossios, Dimitrios Ntelios, Thomas Zegkos, Despoina Parcharidou, Pavlos Rouskas, Sotirios Katranas, Ioannis Papoulidis, Vlasis Ninios, Antonios Ziakas, Georgios K. Efthimiadis   +9 more
wiley   +1 more source

Risk Factors and Predictive Modeling of Occult Choledocholithiasis in Patients with Cholecystolithiasis. [PDF]

Gastroenterol Res Pract
Zhang P, Chen LJ, Liu DF.
europepmc   +1 more source

Clinical Correlates and Heritability of Flow-Mediated Dilation in the Community: The Framingham Heart Study

Circulation, 2004
E. Benjamin, M. Larson, M. Keyes, G. Mitchell, R. Vasan, J. Keaney, B. Lehman, Shuxia Fan, Ewa W Osypiuk, J. Vita   +9 more
semanticscholar   +1 more source

The 9th International RASopathies Symposium

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT The RASopathies are a group of congenital disorders with overlapping clinical manifestations that are caused by pathogenic germline or early somatic variants that result in the hyperactivation of the RAS/mitogen‐activated protein kinase (MAPK) signaling pathway.
Pau Castel, Lisa Schoyer, Beth Stronach, Raya Bogdanova, Anton M. Bennett, Jaishri Blakeley, Miriam Bornhorst, Tammy Bowers, Saskia M. Brachmann, Emma Burkitt‐Wright, Kathryn Chatfield, Alessandro De Luca, Khalil El‐Chammas, Abdul Elkadri, John E. Fortunato, Bruce D. Gelb, Anne Goriely, Karen Gripp, Kassidy Grover, Lindsay Homan, Kenneth A. Kern, Maija Kiuru, Charles (Chuck) Lawson, Yong‐Seok Lee, Frank McCormick, Gina Ney, Cristina Nuevo‐Tapioles, Sara Pardej, Elizabeth I. Pierpont, Julia Plank, Nancy Ratner, Katherine A. Rauen, J. Elliott Robinson, Les Rogers, Sarah E. Sheppard, Keir Shiels, David Stevenson, Dagmar Tiemens, Matthew Traylor, K. Nicole Weaver, Marielle Yohe, Tamar Green   +41 more
wiley   +1 more source

Physical examination-indicated repeat cerclage in singleton pregnancies: a retrospective cohort study. [PDF]

BMC Pregnancy Childbirth
Yang D, Wang L, Ding J, Pan M.
europepmc   +1 more source

Esophageal Dilation [PDF]

Mayo Clinic Proceedings, 1992
openaire   +2 more sources

Differentiating the Clinical and Variant Spectrum of Hardikar Syndrome From Other MED12‐Related Developmental Disorders

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT The rare X‐linked female‐restricted Hardikar syndrome (HDKR, OMIM # 301068) is characterized by multiple congenital anomalies including orofacial clefts, gastrointestinal, genitourinary, and cardiac anomalies, but cognitive and neurobehavioral development is rarely impaired.
Tinne Warmoeskerken, Miel Theunis, Kris Van den Bogaert, Koenraad Devriendt, Jeroen Breckpot   +4 more
wiley   +1 more source

Removal of an over-the-scope clip using balloon dilation. [PDF]

Endoscopy
Lambin T, Leblanc S, Napoleon B, Fumex F, Gincul R, Lepilliez V.   +5 more
europepmc   +1 more source