Results 81 to 90 of about 22,049 (220)
Early onset of homozygous betao-thalassaemia associated with neonatal jaundice. [PDF]
M. Furbetta+5 more
openalex +1 more source
ABSTRACT Glycogen storage disease type III (GSD III) is an inborn error of carbohydrate metabolism with an autosomal recessive inheritance pattern. Phenotypically, patients can manifest a broad clinical spectrum. Most patients affected with GSD IIIA (85%) have a non‐functional GDE enzyme primarily affecting the liver and cardiac/skeletal muscle (Type ...
Nuria Puente‐Ruiz+9 more
wiley +1 more source
Determination the role of risk factor in neonatal jaundice disease at AL- Nasiriya city
Descriptive study was carried out to assess of neonatal jaundice in the sample consist of 150 patients selected from Bent – AL Huda hospital during ( 1- 10 -201 2 ) to ( 1- 10 -2013 ).
ojs_admin
doaj
Neonatal Jaundice and Maternal Oxytocin Infusion [PDF]
D P Davies+4 more
openalex +1 more source
Developmental Profiles of Young Deaf and Hard of Hearing Children and Their Associated Predictors
ABSTRACT Background Concomitant developmental disability is common in deaf and hard of hearing (DHH) children. We describe the early developmental profiles of DHH children and explore factors that may be predictive of these profiles. Methods We report on data from DHH children aged 0–66 months who are participants of a longitudinal child hearing ...
Natalie Zehnwirth+3 more
wiley +1 more source
Objective: The main objective of this study was to determine the prevalence and risk factors of neonatal jaundice in babies born at Westend Hospital in Zimbabwe between January and December 2021.
Chiwoniso Mitchelle Kahiya+2 more
doaj
Hidradenitis Suppurativa Treatment During Pregnancy and Lactation: Navigating Challenges
ABSTRACT Hidradenitis suppurativa (HS), or acne inversa, is a chronic inflammatory skin condition primarily affecting skin folds such as the axilla, groins, and the inframammary, perineal, and perianal regions. It is characterized by painful abscesses, sinus tracts, and scarring.
Laşin Özbek+3 more
wiley +1 more source
Controlled Trial of Phenobarbitone in Neonatal Jaundice [PDF]
G E Levin, G. P. McMullin, Amira Mobarak
openalex +1 more source
Letter: Oxytocin in labour and neonatal jaundice. [PDF]
Sharon Gould+2 more
openalex +1 more source
ABSTRACT Severe alpha‐1 antitrypsin deficiency (AATD) is a rare genetic condition characterised by low systemic levels of alpha‐1 antitrypsin due to its retention in the liver. Consequently, it predisposes individuals to the development of chronic obstructive pulmonary disease and liver cirrhosis.
Joost Boeckmans+4 more
wiley +1 more source