Results 81 to 90 of about 25,566 (257)

Challenges in Diagnosing Central Adrenal Insufficiency in Children: Cortisol‐Stimulating Tests are Safe and Often Required

Clinical Endocrinology, EarlyView.
ABSTRACT Introduction The accuracy and safety of cortisol‐stimulating tests (CSTs) for assessing hypothalamic–pituitary–adrenal (HPA) axis integrity, including the diagnosis of central adrenal insufficiency (CAI), in children remain uncertain. Although these tests can simultaneously evaluate cortisol and growth hormone secretion, the present study ...
Mariana Peduti Halah, Ana Carolina Maia Teodózio, Davi Casale Aragon, Paula Conde Lamparelli Elias, Margaret de Castro, Ayrton Custodio Moreira, Sonir Rauber Antonini   +6 more
wiley   +1 more source

NEONATAL JAUNDICE: THE BENEFITS OF THE ROOMING-IN MODEL FOR THE PROMOTION OF BREASTFEEDING. A REVIEW FROM THE LITERATURE. [PDF]

openIntroduzione: l’ittero neonatale è una manifestazione clinica di bilirubina sierica totale elevata, detta iperbilirubinemia neonatale. Le caratteristiche dell’ittero neonatale includono pelle, sclere e mucose giallastre.
ARDOLINO, DANIELA
core  

Factors associated with neonatal jaundice among neonates admitted to three hospitals in Burao, Somaliland: a facility-based unmatched case-control study

BMC Pediatrics
Background Neonatal jaundice is a common and potentially serious condition affecting newborns worldwide. This study aimed to identify factors associated with neonatal jaundice among neonates admitted to three hospitals in Burao, Somaliland.
Dek Kahin Yosef, Fadumo Osman Ahmed, Barwaqo Saleban Awil, Mohamed Omer Farah, Mohamed Omer Ali   +4 more
doaj   +1 more source

The Spectrum of Congenital Hypogonadotropic Hypogonadism: A 30‐Year Experience at a Tertiary Paediatric Centre

Clinical Endocrinology, EarlyView.
ABSTRACT Congenital hypogonadotropic hypogonadism (CHH) is a rare group of disorders of gonadotropin deficiency, either isolated or as a part of multiple pituitary hormone deficiencies (MPHD). We aimed to describe the spectrum of presentation, diagnosis, and management practices of CHH spanning 30 years at an Australian tertiary paediatric centre. This
Minha Kook, Richard G. McGee, Geoffrey Ambler, Yoon Hi Cho   +3 more
wiley   +1 more source

Predictors of Neonatal Jaundice Admissions: A Comparative Study Between Thai and Myanmar Mothers Residing in Thailand [PDF]

Wimala Eksamut,1 Somsiri Rungamornrat,2 Sudaporn Payakkaraung2 1Master of Nursing Sciences (Pediatric Nursing) (Candidate), Faculty of Nursing, Mahidol University, Bangkok, Thailand; 2Department of Pediatric Nursing, Faculty of Nursing, Mahidol ...
Eksamut W, Payakkaraung S, Rungamornrat S   +2 more
core   +1 more source

Antioxidant status in neonatal jaundice before and after phototherapy [PDF]

, 2015
Background: Neonatal jaundice refers to yellow coloration of the skin and the sclera (whites of the eyes) of newborn babies that result from the accumulation of bilirubin in the skin and mucous membranes.
S Swathi, Sachu Philip, N Bharathy, V Ramesh, A Arun Kumar, C Naveen Kumar, S Ayyappan   +6 more
core   +1 more source

Aetiology of neonatal jaundice in apparently well late-preterm and term neonates at a mission hospital, Southwestern Nigeria

Nigerian Journal of Paediatrics, 2022
Background The knowledge of the aetiology for neonatal jaundice is important in the early detection and effective management of infants with or at risk of severe jaundice before hospital discharge. This study assessed the aetiological factors of neonatal
Alao Michael Abel , Olasinde Yetunde Toyin , Olasinde Yetunde Toyin , Tongo Olukemi Oluwatoyin , Adeleke Olumide Thomas , Slusher Tina Marye   +5 more
doaj  

USP34 Haploinsufficiency as a Cause of Neurodevelopmental Phenotypes

Clinical Genetics, EarlyView.
Heterozygous loss‐of‐function variants in USP34 cause a novel neurodevelopmental disorder characterized by global developmental delay, speech impairment, autism, hypotonia, craniofacial dysmorphism, and distal limb anomalies. Disrupted Wnt/β‐catenin signaling via reduced Axin stabilization refines gene‐specific contributions within 2p15p16.1 ...
Helena Wigoda, Amjad Khan, Bryce A. Mendelsohn, Noriko Miyake, Nobuhiko Okamoto, Naomichi Matsumoto, Patricia J. C. Knijnenburg, Johanna M. van Hagen, Jiddeke van de Kamp, Quinten Waisfisz, Bryn D. Webb   +10 more
wiley   +1 more source

Research Progress of Neonatal Jaundice 2013-2023: a Bibliometric Analysis [PDF]

Background: Jaundice or neonatal jaundice is a problem that occurs in neonates, especially in the first week of life, which is caused by the accumulation of bilirubin that exceeds the threshold in the blood and tissues.
Ariyanti, Ida, Amelia, Rizky, Martanti, Listyaning Eko, Rofi'ah, Siti   +3 more
core   +1 more source

Neurodevelopmental Phenotypes and Brain Anomalies in Individuals With Heterozygous SEMA6A Variants

Clinical Genetics, EarlyView.
SEMA6A plays a role in cell migration and axon guidance in the developing central nervous system. Phenotypes seen in eleven individuals heterozygous for SEMA6A variants included developmental delay, intellectual disability, autism/autistic behaviors, behavioral abnormalities, attention disorders, hypotonia, and brain anomalies.
Evan Burchfiel, Xiaonan Zhao, Nichole M. Owen, Tia Gordon, Mahshid S. Azamian, Eric C. Kao, Fan Xia, Xi Luo, Jill A. Rosenfeld, Seema R. Lalani, Allison P. Ortega, Steven B. Bleyl, Florence Petit, Sulekha Rajagopolan, Bénédicte Demeer, Meredith K. Gillespie, Lijia Huang, Matthew Osmond, Kym M. Boycott, Kyra E. Stuurman, Marjon A. van Slegtenhorst, Haley Soller, Céline Jost, Aurore Garde, Hana Safraou, Laurence Faivre, Victor Faundes, Daryl A. Scott   +27 more
wiley   +1 more source