Results 121 to 130 of about 358,326 (257)

Determination the role of risk factor in neonatal jaundice disease at AL- Nasiriya city

open access: yesمجلة علوم ذي قار, 2019
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  

Maternal care practices and health-seeking behaviour for neonatal jaundice in Basawa Community, Zaria, Northwestern Nigeria

open access: yes, 2019
Neonatal jaundice (NNJ) is a common condition that occurs in newborns which is preventable and also easily treatable. However, delay in the presentation of infants with jaundice at the hospital is associated with increased morbidity and mortality.
Igboanusi, C.J.C.   +4 more
core   +1 more source

Vaccinations During Pregnancy Protect the Mother–Infant Dyad and Are Generally Safe

open access: yesActa Paediatrica, Volume 115, Issue 11, Page 2380-2388, November 2026.
ABSTRACT Aim Vaccination in pregnancy has a critical impact on mothers, foetuses and infants. The aim of this paper was to summarise key points presented by experts attending the 12th Maria Delivoria‐Papadopoulos Perinatal Symposium in March 2025 and further expand and update them.
Ariadne Malamitsi‐Puchner   +2 more
wiley   +1 more source

NEONATAL JAUNDICE IN HYPERBILIRUBINEMIC INFANTS

open access: yes, 2022
Introduction: Hyperbilirubinemia is a problem that often occurs in newborns. In pathological conditions, infants experience jaundice throughout the body or degrees three to six experiencing hyperbilirubinemia > 12 mg/dl.
Sari, Dita Novita   +3 more
core  

Surviving Males With PORCN Variants: Expanding the Clinical, Molecular, and Mechanistic Spectrum

open access: yesClinical Genetics, Volume 110, Issue 5, Page 605-615, November 2026.
Pathogenic PORCN variants are compatible with male survival in both mosaic and non‐mosaic states, expanding the FDH/PONGOS spectrum and improving diagnosis and genetic counseling. ABSTRACT Pathogenic variants in PORCN cause focal dermal hypoplasia (FDH/Goltz syndrome), an X‐linked dominant disorder historically considered lethal in males, with milder ...
Lucía Miranda‐Alcaraz   +23 more
wiley   +1 more source

Recent advances in polyendocrine metabolic ovarian syndrome, formerly polycystic ovary syndrome, with emphasis on endocrine and metabolic dysfunction and cardiovascular risk

open access: yesJournal of Internal Medicine, Volume 300, Issue 5, Page 590-609, November 2026.
Abstract Polyendocrine metabolic ovarian syndrome (PMOS), previously known as polycystic ovary syndrome, affects 10%–13% of women of reproductive age and remains underdiagnosed despite its substantial health burden. The introduction of the new PMOS nomenclature in 2026 reflects a fundamental shift in understanding the condition as a lifelong endocrine ...
Maria Forslund   +5 more
wiley   +1 more source

Determinants of Early Neonatal Weight Loss in Historical Swiss Maternity Hospital Records

open access: yesAmerican Journal of Human Biology, Volume 38, Issue 10, October 2026.
ABSTRACT Objective Early neonatal weight loss is an aspect of neonatal adaptation influenced by maternal, nutritional, and perinatal factors. Determinants of early neonatal weight loss in historical populations remain poorly understood. This study investigated determinants of neonatal weight loss as an early postnatal adaptation phenotype using Swiss ...
Anton Nagaroor   +3 more
wiley   +1 more source

Neonatal adrenal hemorrhage presenting as late onset neonatal jaundice

open access: yes, 2009
Clinical manifestations of adrenal hemorrhage vary depending on the degree and rate of hemorrhage, as well as the amount of adrenal cortex compromised by hemorrhage.
Ahmad Nisar   +3 more
core  

Relationship Between Low Birth Weight and Neonatal Jaundice: Retrospective Case-Control Study at Wates Regional Hospital

open access: yes
Introduction: Neonatal mortality is a critical indicator of public health and reflects the quality of maternal and neonatal healthcare services in a country. Low birth weight (LBW) and neonatal jaundice are among the leading causes of neonatal morbidity.
Handayani, Sri, Emy Siti Lestari
core   +1 more source

Histidine Supplementation Stabilizes Hearing and Vision and Improves Growth in HARS1‐Related Autosomal Recessive Disorder Associated With Usher‐Like Symptoms

open access: yesAmerican Journal of Medical Genetics Part A, Volume 200, Issue 10, Page 2289-2308, October 2026.
ABSTRACT Autosomal recessive HARS1‐related disorder (originally described as Usher syndrome type 3B) caused by a homozygous Y454S variant in the histidyl‐tRNA synthetase gene (HARS1) is characterized by progressive sensorineural hearing and vision loss and respiratory deterioration with risk for sudden death following febrile illnesses.
Victoria Mok Siu   +23 more
wiley   +1 more source

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