Results 61 to 70 of about 387,299 (307)

Abordaje quirúrgico por mínima invasión en disfagia lusoria

Archivos de Cardiología de México
La arteria lusoria tiene una prevalencia del 0.5% al 2% en la población general. Se trata de un arco aórtico izquierdo con arteria subclavia derecha aberrante, resulta de la regresión del cuarto arco derecho y la aorta dorsal derecha proximal.
Carlos Alcántara-Noguez, Desireé Leines-Castelán, Aarón E. Buenabad-Hernández, Alejandra Contreras-Ramos, Sergio Ruiz-González, Patricia Romero-Cárdenas, Alejandro Bolio-Cerdán   +6 more
doaj   +1 more source

Umbilical Cord Arterial Blood Gas and Apgar Score: Who Is at Higher Risk? [PDF]

Iranian Journal of Neonatology, 2019
Background: Fetal asphyxia and the consequent neurological damages could be avoided if the risk factors are controlled at earlier stages. Umbilical cord arterial blood gas (UCABG) seems to be related to the Apgar scores, as well as the neonatal morbidity
Elham Mobasheri, Marzieh Savarrakhsh, Seyyed Mohsen Hosseininejad, Ehsan Alaee   +3 more
doaj   +1 more source

Deubiquitination of Vangl by USP6 and USP32 Regulates Planar Cell Polarity Signaling

Advanced Science, EarlyView.
Compartment‐specific deubiquitination controls Vangl dosage and planar cell polarity signaling. USP6 and USP32 regulate distinct subcellular pools of Vangl by removing distinct ubiquitin modifications from Vangl proteins. This regulatory mechanism safeguards PCP‐dependent embryonic morphogenesis, while aberrant USP32‐dependent stabilization of VANGL ...
Fangzi Zha, Di Feng, Ziru Xue, Zhiying Liu, Xiaochen Lin, Zhe Wang, Ling Xu, Jasper Fuk Woo Chan, Martin Cheung, Michael Shing Yan Huen, Yusong Guo, Kui Ming Chan, Yun Liu, Bo Gao   +13 more
wiley   +1 more source

Fetal lung lesions diagnosis: the crucial role of ultrasonography [PDF]

, 2009
Fetal lung lesions may cause significant effects of mass and may evolve into a non-immune hydrops and lead to the death of the fetus or the child. Treatment options for these severely affected infants are constantly evolving.
Maiello, Monica, Dinatale, Angela, Palermo, Mariarosaria, Carrara, Sabina, Esposito, Nunzia, Pedata, Rosa, Cavaliere, Alessandra, Ermito, Santina   +7 more
core   +1 more source

Pattern and risk factors of cryptorchidism in Gorgan, northern Iran

مجله دانشگاه علوم پزشکی گرگان, 2014
Background and Objective: Cryptorchidism or undescending testis is a developmental defect and occurred in 2-4% of male newborns. This study was done to determine the pattern and risk factors of cryptorchidism in Gorgan, northern Iran.
Mirfazeli A, Kavianyn N, Vakili MA, Tajari HA, Golalipour MJ   +4 more
doaj  

Late Total Cavopulmonary Connection in Adolescents and Adults: Narrative Review of Patient Selection and Outcomes

Journal of Cardiovascular Development and Disease
Background: Although most patients with univentricular physiology undergo staged palliation during childhood, a small subset reaches adolescence or adulthood without complete cavopulmonary connection. The role of late total cavopulmonary connection (TCPC)
Hichem Sakhi, Sébastien Hascoët, Emre Belli, Sarah Cohen   +3 more
doaj   +1 more source

TECTB Variants Reveal Tectorial Membrane Vulnerability in Dominant Non‐Syndromic Hearing Loss

Advanced Science, EarlyView.
TECTB is a non‐collagenous protein of the tectorial membrane – an extracellular matrix of the cochlea. This study identifies dominant missense variants in TECTB linked to human hereditary deafness in two unrelated families. Genetically engineered mice homozygous for one of the variants are profoundly deaf, whereas heterozygous mice have normal hearing ...
Evan B. Hale, Barbara Vona, Richard J. Goodyear, Richard T. Osgood, Jun Shen, Sami S. Amr, Karen Mojica, Michaela A. H. Hofrichter, Jörg Schröder, Sophie Flandin, Paul Gratias, Ricardo Vera‐Monroy, Katherine Callahan, Kerry L. Gudlewski, Rolen Quadros, Masato Ohtsuka, JoAnn McGee, Edward J. Walsh, Cynthia C. Morton, Thomas Haaf, Channabasavaiah Gurumurthy, James E. Saunders, Guy P. Richardson, Artur A. Indzhykulian   +23 more
wiley   +1 more source

Ethnical Variations in the Incidence of Congenital Heart Defects in Gorgan, Northern Iran: A Single-Center Study

Journal of Tehran University Heart Center, 2015
Background: Congenital heart disease (CHD) is the most common congenital anomaly in newborns. This study was performed to determine the live birth incidence of CHD by ethnicity and sex in Gorgan, Northern Iran.
Bagher Nikyar, Maliheh Sedehi, Mostafa Qorbani, Arash Nikyar, MohammadJafar Golalipour   +4 more
doaj  

3 year old with chronic wet cough : Intralobar Bronchopulmonary sequestration [PDF]

, 2016
Bronchopulmonary sequestration (BPS) is a rare congenital foregut anomaly of the lung, consisting of nonfunctioning primitive tissue that does not communicate with the healthy tracheobronchial tree.
Micallef, S.P., Sammut, Patrick, DeGiovanni, Joseph V., Grech, Victor E.   +3 more
core  

TH/TRs–COL11A2 Axis Mediates Loss of a Differentiated Astrocyte State in Hypogyrified Brains

Advanced Science, EarlyView.
Using a gyrencephalic congenital hypothyroidism pig model, this study reveals cerebral atrophy and cortical hypogyrification. Single‐cell sequencing identifies astrocytes as major TH‐responsive cells, with the COL11A2‐enriched Astro‐2 state nearly absent.
Ying Zhang, Xiao Wang, Hongyan Ma, Pengcheng Lyu, Shuangjie Tian, Ruojun Zong, Jiani Chen, Gang Ren, Yongjiang Yang, Zichen Yang, Guosong Qin, Naishi Li, Yanfang Wang, Jianwei Jiao, Jianguo Zhao   +14 more
wiley   +1 more source