Results 81 to 90 of about 1,301,542 (365)

FAKTOR­-FAKTOR RISIKO TERJADINYA ASFIKSIA NEONATORUM DI RSD JOMBANG PERIODE 1 JANUARI ­- 31 DESEMBER 2007 [PDF]

open access: yes, 2009
Neonatal Asphyxia is an emergency condition when the baby failed to breath spontaneously and regularly after they were born. Neonatal asphyxia remains the main cause of neonatal mortality as well as permanent neurological abnormality.
SUNDARI TIKA, TRI
core  

Skin calcium deposits in primary familial brain calcification: A novel potential biomarker

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
Abstract Objective Primary Familial Brain Calcification (PFBC) is a rare neurodegenerative disorder characterized by small vessel calcifications in the basal ganglia. PFBC is caused by pathogenic variants in different genes and its physiopathology is still largely unknown. Skin vascular calcifications have been detected in single PFBC cases, suggesting
Aron Emmi   +8 more
wiley   +1 more source

Outcomes and related factors in a cohort of infants born in Taiwan over a period of five years (2007–2011) with borderline viability

open access: yesJournal of the Formosan Medical Association, 2018
Background: Advances in perinatal and neonatal care have increased the survival of extremely preterm infants, but the viability limit is still debated. Here we assess the survival, neonatal morbidity, and neurodevelopmental outcomes at 2 years of age of ...
Jui-Hsing Chang   +3 more
doaj  

Premature Menopause

open access: yesAnnals of Medical and Health Sciences Research, 2013
Premature menopause affects 1% of women under the age of 40 years. The women are at risk of premature death, neurological diseases, psychosexual dysfunction, mood disorders, osteoporosis, ischemic heart disease and infertility. There is need to use simplified protocols and improved techniques in oocyte donation to achieve pregnancy and mother a baby in
Okeke, TC, Anyaehie, UB, Ezenyeaku, CC
openaire   +4 more sources

Novel Phenotypes and Deep Intronic Variant Expand TH‐Associated Dopa‐Responsive Dystonia Spectrum

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Approximately 20% of dopa‐responsive dystonia (DRD) cases remain genetically unresolved. Using whole‐genome sequencing, we identified two TH variants in a young DRD patient, including a novel deep intronic variant. Minigene assays confirmed that this variant causes aberrant splicing.
Xiaosheng Zheng   +6 more
wiley   +1 more source

A Review of Non-Pharmacological Treatments for Pain Management in Newborn Infants

open access: yesChildren, 2018
Pain is a major problem in sick newborn infants, especially for those needing intensive care. Pharmacological pain relief is the most commonly used, but might be ineffective and has side effects, including long-term neurodevelopmental sequelae.
Avneet K. Mangat   +4 more
doaj   +1 more source

Premature Unilateral Ripening in Euonymus alatus: Two Hits Leave(s) a Red Face [PDF]

open access: yesarXiv, 2017
An empirical 2-hit hypothesis is presented to account for premature and unilateral ripening in Euonymus alatus.
arxiv  

TREATMENT OF PREMATURITY [PDF]

open access: yesJAMA: The Journal of the American Medical Association, 1918
It is my purpose to present in this paper the method and the results of the treatment of premature infants in the University of Minnesota Hospital. The material studied includes sixty prematurely born infants, all being born at, or otherwise admitted to, the clinic from September, 1914, when the department of pediatrics assumed charge of the new-born ...
openaire   +2 more sources

Phase 1, First‐In‐Human, Single‐/Multiple‐Ascending Dose Study of Iluzanebart in Healthy Volunteers

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective To evaluate the safety, tolerability, pharmacokinetics, and pharmacodynamics of iluzanebart, a fully human monoclonal antibody TREM2 (triggering receptor expressed on myeloid cells 2) agonist, after single‐ (SAD) and multiple‐ascending‐dose (MAD) administration.
Andreas Meier   +8 more
wiley   +1 more source

Homocysteine and Risk of Premature Coronary Heart Disease

open access: yesAlbanian Journal of Trauma and Emergency Surgery, 2020
Background: Homocystinuria is a rare autosomal recessive disease complicated by early and aggressive occlusive arterial disease. This may be related to the grossly increased homocysteine concentrations seen in this disease.
Lutfi Zylbeari   +9 more
doaj   +1 more source

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