Results 11 to 20 of about 164,501 (266)

Multifactorial origin of pulmonary hypertension in a child with congenital heart disease, Down syndrome, and BMPR‐2 mutation

open access: yesPulmonary Circulation, 2021
A late preterm infant had pulmonary hypertension caused by a variety of mechanisms leading to complex management. This child had complete atrioventricular septal defect associated with mild left ventricular hypoplasia and Down syndrome diagnosed ...
Fanny Bajolle   +3 more
doaj   +1 more source

Multiple congenital malformation in a Simental female calf: a case report

open access: yesVeterinární Medicína, 2010
Congenital anomalies in offspring of natural breedings are often a result of environmental factors, genetic factors, or both. A 21-day-old male Simental female calf was submitted to our clinic with abnormal severe green mucoid nasal discharge from both ...
O. Smolec   +5 more
doaj   +1 more source

Spontaneous Closure of the Arterial Duct after Transcatheter Closure Attempt in Preterm Infants

open access: yesChildren, 2021
(1) Background: Transcatheter closure of the patent arterial duct (TCPDA) in preterm infants is an emerging procedure. Patent arterial duct (PDA) spontaneous closure after failed TCPDA attempts is seen but reasons and outcomes are not reported; (2 ...
Mathilde Méot   +10 more
doaj   +1 more source

Retrospective study on growth in infants with isolated Robin sequence treated with the Tuebingen Palate Plate

open access: yesOrphanet Journal of Rare Diseases, 2021
Background Children with Robin sequence (RS) are at risk of growth failure, mainly due to their increased work of breathing and feeding difficulties. Various conservative and surgical treatment approaches exist, but their impact on weight gain has not ...
Cornelia Wiechers   +10 more
doaj   +1 more source

Long-term outcomes of transcatheter Potts shunt in children with suprasystemic pulmonary arterial hypertension

open access: yesFrontiers in Cardiovascular Medicine, 2022
BackgroundTranscatheter Potts shunt (TPS) is a palliation alternative for children with severe pulmonary arterial hypertension (PAH). Debates on the long-term outcomes remain unsolved.ObjectivesTo evaluate long-term clinical and procedural outcomes of ...
Raymond N. Haddad   +6 more
doaj   +1 more source

Comparison of Placental Histopathological Findings with Good and Adverse Neonatal Outcomes- A Prospective Observational Study [PDF]

open access: yesIndian Journal of Neonatal Medicine and Research, 2022
Introduction: The placenta plays a crucial role in the growth and survival of foetus by performing most of the vital functions for the foetus before delivery.
Nidhi Sachan   +2 more
doaj   +1 more source

Cocktail effect of Profenophos and Abamectin on tadpoles of Asian Common Toad (Duttaphrynus melanostictus)

open access: yesCeylon Journal of Science, 2018
Farmers mix two or more pesticides as mixing saves the spraying time and the labour cost and also with the idea that it increases the efficiency. The cocktail effect of two agrochemicals, profenophos and abamectin, was tested on the tadpoles of the Asian
R. R. P. Y. K. Rathanayaka   +1 more
doaj   +1 more source

Actual epidemiological profile and management of central nervous system (CNS) malformations in a neurosurgery department in sub-Saharan Africa

open access: yesArchives of Pediatric Neurosurgery, 2023
Introduction: Central Nervous System (CNS) malformations usually leave the family in disarray and doctors’ staff powerless. In developed countries, the rigorous application of preventive measures has contributed to a significant reduction incidence of ...
Denlewende Sylvain Zabsonre   +7 more
doaj   +1 more source

Congenital anomalies of the urethra

open access: yesВестник урологии, 2021
Congenital anomalies of the urethra are insufficiently covered in the literature, except for hypospadias and epispadias. Therefore, there is a significant gap in information on the diagnosis, classification and management of patients with such anomalies ...
M. I Katibov, A. B. Bogdanov
doaj   +1 more source

RAB23 coordinates early osteogenesis by repressing FGF10-pERK1/2 and GLI1

open access: yeseLife, 2020
Mutations in the gene encoding Ras-associated binding protein 23 (RAB23) cause Carpenter Syndrome, which is characterized by multiple developmental abnormalities including polysyndactyly and defects in skull morphogenesis.
Md Rakibul Hasan   +5 more
doaj   +1 more source

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