Results 61 to 70 of about 88,012 (270)

Revesz syndrome

open access: yesRevista Brasileira de Oftalmologia, 2015
Revesz syndrome is a rare variant of dyskeratosis congenita and is characterized by bilateral exudative retinopathy, alterations in the anterior ocular segment, intrauterine growth retardation, fine sparse hair, reticulate skin pigmentation, bone marrow ...
Dayane Cristine Issaho   +4 more
doaj   +1 more source

Genetics Crime and Justice [PDF]

open access: yes, 2015
This review is unashamedly from the perspective of English law because busy United Kingdom criminal law solicitors and barristers mostly wish to know what the law states, which case is a precedent case and whether the author has provided up-to-date legal
Ramage, Sally
core  

The functions of postpartum depression [PDF]

open access: yes, 1999
Evolutionary approaches to parental care suggest that parents will not automatically invest in all offspring, and should reduce or eliminate investment in their children if the costs outweigh the benefits.
Hagen, Edward
core   +2 more sources

Prenatal betamethasone–postnatal N‐methyl‐D‐aspartic acid model of spasms: Update on mechanisms and treatments

open access: yesEpilepsia Open, EarlyView.
Abstract Infantile epilepsy spasms syndrome (IESS), formerly known as infantile spasms or West Syndrome, is a severe epilepsy syndrome affecting about 3 in 10,000 newborns in the United States. Characterized by clusters of epileptic spasms, interictal hypsarrhythmia, and developmental delays, IESS has diverse causes, including structural‐metabolic ...
Kayla Vieira   +5 more
wiley   +1 more source

Vitamin B12 deficiency as a cause of severe neurological symptoms in breast fed infant – a case report

open access: yesItalian Journal of Pediatrics, 2020
Background Vitamin B12 (cobalamin, cbl) deficiency in children is rare and may occurs in exclusively breast fed infants of mothers on vegetarian or vegan diet with lack of appropriate supplementation.
Cezary Dubaj   +2 more
doaj   +1 more source

Characterization of a rare analphoid supernumerary marker chromosome in mosaic [PDF]

open access: yes, 2015
publicado em: Chromosome Research. 2015;23(Suppl 1):67-8. doi:10.1007/s10577-015-9476-6Analphoid supernumerary marker chromosomes (SMCs) are a rare subclass of SMCs C-band-negative and devoid of alpha-satellite DNA.
Alves, C.   +6 more
core  

Effects of scopolamine on matching to sample paradigm and related tests in human subjects [PDF]

open access: yes, 2003
This was a double-blind placebo-controlled study with a cross-over design to examine the effects of scopolamine on cognitive functions in young healthy subjects.
Adam, M.   +6 more
core   +1 more source

Ketogenic diet for infantile epileptic spasms

open access: yesEpilepsia Open, EarlyView.
Abstract Approximately half of all cases of Infantile Epileptic Spasms Syndrome (IESS) do not respond to vigabatrin and hormonal therapies. There is no clear consensus as to the second‐line therapy for IESS. Ketogenic diet (KD) has emerged as an effective treatment for certain drug‐resistant epilepsies and in many cases of IESS.
Morris H. Scantlebury   +3 more
wiley   +1 more source

Detection of Psychomotor Retardation in Youth Depression: A Machine Learning Approach to Kinematic Analysis of Handwriting

open access: yesApplied Sciences
Depressive disorders significantly impact individuals worldwide, including children and adolescents. Despite their widespread occurrence, early and precise diagnosis of depressive disorders remains a complex and challenging task, particularly in younger ...
Vladimir Džepina   +6 more
doaj   +1 more source

Development of bipedal and quadrupedal locomotion in humans from a dynamical systems perspective [PDF]

open access: yes, 2012
The first phase in the development 0f locomotion, pr,öary variability would occur in normal fetuses and infants, and those with Uner Tan syndrome. The neural networks for quadrupedal locomotion have apparently been transmitted epigenetically through many
Tan, Prof. Dr. Uner
core   +2 more sources

Home - About - Disclaimer - Privacy