Results 61 to 70 of about 343,621 (301)

Changes of smooth muscle contractile filaments in small bowel atresia

, 2012
AIM: To investigate morphological changes of intestinal smooth muscle contractile fibres in small bowel atresia patients. METHODS: Resected small bowel specimens from small bowel atresia patients (n = 12) were divided into three sections (proximal ...
Rolle, Udo, Metzger, Roman, Fiegel, Henning C., Gfrörer, Stefan, Ramachandran, Priya   +4 more
core   +1 more source

Long-term healthcare utilization, medical cost, and societal cost in adult congenital heart disease

, 2020
Objective: Cost-of-illness studies in Adult Congenital Heart Disease (ACHD) have mainly been limited to hospitalizations. This is the first paper to provide a comprehensive overview from a societal perspective including inpatient and outpatient medical ...
Annemans, Lieven, Moniotte, S., Ombelet, F., Moons, Philip, Budts, Werner, de Hosson, M., Marelli, A., De Backer, Julie, Annemans, L., Van Bulck, Liesbet, Willems, R., de Hosson, Michèle, Goossens, E., Moons Julie De Backer, Philip, Budts, W., Van Bulck, L., De Groote, Katya, Goossens, Eva, Marelli, Arianne, De Groote, K., Willems, Ruben, Ombelet, Fouke, De Backer, J., Moniotte, Stéphane, Moons, Philip,   +24 more
core   +2 more sources

Changes in Near-Infrared Spectroscopy After Congenital Cyanotic Heart Surgery

Frontiers in Pediatrics, 2018
BackgroundSince oxygen saturation from pulse oximetry (SpO2) and partial pressure of arterial oxygen (PaO2) are observed to improve immediately after surgical correction of cyanotic congenital heart disease (CHD), we postulate that cerebral (CrO2) and ...
Judith Ju-Ming Wong, Judith Ju-Ming Wong, Ching Kit Chen, Rajesh Babu Moorakonda, Rajesh Babu Moorakonda, Olivia Wijeweera, Tracy Yi Shuen Tan, Masakazu Nakao, John Carson Allen, Tsee Foong Loh, Tsee Foong Loh, Jan Hau Lee, Jan Hau Lee   +12 more
doaj   +1 more source

Sertraline Treatment Can Mimic Niemann‐Pick Type C Biomarker Profile: A Diagnostic Pitfall

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Background Oxysterols (cholestane‐3β,5α,6β‐triol and 7‐ketocholesterol) and N‐palmitoyl‐O‐phosphocholineserine (PPCS) are sensitive biomarkers for Niemann‐Pick disease type C (NPC) screening. However, false‐positive results occur, with a biomarker profile suggestive of NPC despite the absence of pathogenic variants in genes involved in NPC or ...
Maria Makrygianni, Cecile Pagan, Antony Citterio‐Quentin, Isabelle Rouvet, Giulia Dingeo, Cyril Hanin, Claudine Laurent‐Levinson, Samia Pichard, Bénédicte Héron, Clément Gourguechon, Daniele Mandia, Jerome Guitton, Carole Lacout, Nicolas Schleinitz, Florient Potier, Olivier Flabeau, Elsa Besse‐Pinot, Foudil Lamari, Magali Pettazzoni, Yann Nadjar   +19 more
wiley   +1 more source

Changes in the Cath Lab in the Treatment of Adult Patients with Congenital Heart Disease: A 12-Year Experience in a Single Referral Center with the Establishment of a Dedicated Working Group

, 2023
Background: Adults with congenital heart disease (ACHD) are a growing population needing ongoing care. The aim of this study was to investigate if a dedicated ACHD team impacted the timing and indication of invasive cardiology procedures in these ...
Francesca Fanisio, Elettra Pomiato, Maria Giulia Gagliardi, Massimiliano Raponi, Paolo Guccione, Rosaria Barracano, Lorenzo Galletti, Rosalinda Palmieri, Roberto Formigari, Mario Panebianco, Marco Alfonso Perrone   +10 more
core   +1 more source

Recurrent Hypothermia and Autonomic Dysfunction Secondary to Shapiro Syndrome

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT A 44‐year‐old man presented with recurrent hypothermia, diaphoresis and hypertension. Extensive investigation for infectious, inflammatory, metabolic and endocrine aetiologies was negative. MR scan of the brain demonstrated no lesions but revealed callosal dysgenesis, consistent with Shapiro syndrome.
Naveen Kumar, Jeremy Johnson, Susanne Watkins, Eoin Mulroy   +3 more
wiley   +1 more source

Congenital spondylolytic spondylolisthesis of the cervical spine: A case report and literature review

Radiology Case Reports, 2022
Congenital spondyloytic spondylolisthesis (CSS) is characterized as a pars-interarticularis well-corticated cleft with antherolithesis. The presence of spina bifida and vertebral dysplastic changes corroborate the possibility of a congenital etiology. It
Imad-eddine Sahri, MD, Zakaria Chandid Tlemcani, MD, Elmehdi Hakkou, MD, Oudrhiri Mohammed yassaad, MD, Elouhabi Abdessamad, MD   +4 more
doaj   +1 more source

A 17 Year Old With Developmental Delay Presenting With Increasing Confusion and Imbalance

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Methylmalonic acidemia is an autosomal recessive genetic disorder primarily caused by defects in methylmalonyl‐CoA mutase and cobalamin (vitamin B12) metabolism. These defects disrupt the tricarboxylic acid cycle and oxidative phosphorylation, leading to the abnormal accumulation of metabolic products such as methylmalonic acid, propionic acid,
Wei Zhao, Yingli Zhang, Hongliang Zheng
wiley   +1 more source

Isolated congenital interruption of the right interlobar pulmonary artery with unilateral interstitial lung abnormality

Respiratory Medicine Case Reports, 2022
We report a case of an isolated congenital interruption of the right interlobar pulmonary artery with unilateral interstitial lung abnormality. 3D-CT with enhancement showed absent right interlobar pulmonary artery without any other abnormalities of the ...
Mitsukuni Sakabe, Kazunori Tobino, Kazuki Uchida, Yosuke Murakami, Yuri Hiramatsu, Hiroaki Ota, Takafumi Kawabata   +6 more
doaj   +1 more source

White Matter Microstructural Abnormalities in Neonatal Onset Genetic Epilepsy

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Recent evidence indicates that epilepsy is associated with abnormal white matter. If seizures alter white matter, then the impact upon network function, epileptogenesis, and cognition could be pronounced in neonates undergoing rapid developmental myelination. Neonates with epilepsy due to nonstructural genetic causes provide a unique
Amanda G. Sandoval Karamian, Tianjia Zhu, Hao Huang, Shavonne L. Massey, Mark P. Fitzgerald, Darshana Parikh, Arastoo Vossough, Ingo Helbig, Nicholas S. Abend   +8 more
wiley   +1 more source