Results 251 to 260 of about 140,126 (358)

Transplantation of the liver in human subjects [PDF]

, 1974
Putnam, CW, Starzl, TE
core  

Mitral atresia

The Journal of Thoracic and Cardiovascular Surgery, 1979
openaire   +2 more sources

A Rational Approach to Pharmacotherapy in Pregnancy

The Journal of Clinical Pharmacology, Volume 66, Issue 1, January 2026.
Abstract Most pregnant individuals are exposed to at least one medication, whether prescription or over the counter, during pregnancy. Despite the ubiquity of medication use in pregnancy, there remains no standardized framework to guide clinicians in selecting the most appropriate pharmacotherapy that balances maternal needs with fetal safety. This gap
Gregory W. Kirschen, Kevin Watt, Ahizechukwu C. Eke   +2 more
wiley   +1 more source

USP9X-triggered ferroptosis mediates follicular atresia via deubiquitinating Beclin1 in chicken. [PDF]

J Anim Sci Biotechnol
Chen Y, Wang W, Cui C, Zhang Y, Li Z, Yin H, Han S.   +6 more
europepmc   +1 more source

Operative implications of preduodenal portal vein [PDF]

, 1979
Lilly, JR, Starzl, TE
core  

Pyloric atresia.

The Turkish journal of pediatrics, 1985
M K Cağlar, M Ceyhan, U Dilmen, D A Senses   +3 more
openaire   +2 more sources

Comparison of Three Different Staging Systems Capable of Predicting the Severity of Congenital Lower Urinary Tract Obstruction (LUTO) and Its Prognosis

Journal of Clinical Ultrasound, Volume 54, Issue 1, Page 177-185, January 2026.
The Ruano's proposed prenatal staging system for LUTO seems to offer a more comprehensive stratification of different severities of fetal LUTO as well as a guidance for potential prenatal therapy based on four stages. ABSTRACT Lower urinary tract obstruction (LUTO) is a rare but severe fetal condition associated with significant morbidity and long‐term
Ugo Maria Pierucci, Irene Paraboschi, Matthieu Peycelon, Chryso P. Katsoufis, Alireza Alam, Gabriele Tonni, Mark D. Kilby, Gloria Pelizzo, Rodrigo Ruano   +8 more
wiley   +1 more source

Esophageal atresia with and without tracheoesophageal fistula: a 2016-2024 single-center cohort study in Saudi Arabia stratified by gap length. [PDF]

World J Pediatr Surg
Ali K, Alsabty NS, Altuwaym A, Al Jadaan S, Al Namshan M, Alharbi N, Homedi A, Ali I, Alsaif S.   +8 more
europepmc   +1 more source

Jaundice in babies: implications for community screening for biliary atresia

, 1995
Déirdre Kelly, A Stanton
openalex   +2 more sources

Holocarboxylase Synthetase Deficiency: A Second Case Report With Neonatal Cholestatic Liver Disease

JIMD Reports, Volume 67, Issue 1, January 2026.
ABSTRACT Holocarboxylase synthetase deficiency is an autosomal recessive inborn error of metabolism characterised by life‐threatening metabolic acidosis, ketoacidosis and hyperammonaemia through reduced biotin‐dependent carboxylase activity. We report the presentation of a Polynesian neonate with severe metabolic acidosis secondary to holocarboxylase ...
Sophie Manoy, Claire Murray, Matthew Lynch, Tahlee Minto, Kelvin Choo, Carolyn Bursle, Michelle Lipke, Jim McGill, Anita Inwood, David Coman   +9 more
wiley   +1 more source