Results 141 to 150 of about 21,000,838 (302)
Delayed Recognition of Maternal G6PD Heterozygous Status Across Prenatal and Newborn Care Interfaces
ABSTRACT Glucose‐6‐phosphate dehydrogenase (G6PD) deficiency is the most common red blood cell enzymatic disorder worldwide. Although many heterozygotes are asymptomatic, affected neonates have an increased risk for hyperbilirubinemia and related complications.
Mona M. Makhamreh +5 more
wiley +1 more source
New Mexico Lobo, Volume 039, No 9, 10/14/1936
New Mexico Lobo, Volume 039, No 9, 10/14 ...
University of New Mexico
core
Methane Activation by B5+ Toward a CB5H2+ Isomer Containing a Planar Tetracoordinate Carbon Atom
Methane activation by B5+ yields CB5H2+ through H2 elimination. Electronic‐structure calculations connect the nascent dehydrogenation product to a low‐lying isomer containing a planar tetracoordinate carbon atom. ABSTRACT Planar tetracoordinate carbon (ptC) motifs have been identified predominantly in the global‐minimum structures of gas‐phase clusters
Qin‐Wei Zhang +11 more
wiley +2 more sources
Genetic Variation in ADHD‐Related Risk Genes in an Indigenous Population of the Amazon
ABSTRACT Attention‐Deficit/Hyperactivity Disorder (ADHD) is a highly heritable neurodevelopmental disorder; however, its genetic architecture remains poorly explored in Indigenous populations. This study aimed to analyze and characterize genetic variation in 11 genes (ADGRL3, CDH8, DCC, DUSP6, FOXP1, FOXP2, MEF2C, PCDH7, SEMA6D, SORCS3, and ST3GAL3 ...
Hirlesson Paixão de Matos +11 more
wiley +1 more source
New Mexico Lobo, Volume 058, No 42, 1/11/1955
New Mexico Lobo, Volume 058, No 42, 1/11 ...
University of New Mexico
core
The Role of Glutamatergic and Dopaminergic Genes in Resistant Schizophrenia: A Systematic Review
ABSTRACT Psychosis is a heterogeneous disorder, with approximately one‐third of patients experiencing treatment resistance, predominantly among individuals diagnosed with Schizophrenia. Treatment‐resistant schizophrenia (TRS) may stem from a distinct biological signature, involving abnormalities in the dopaminergic and glutamatergic systems.
Maria Teresa Moreno‐Calle +3 more
wiley +1 more source
New Mexico Lobo, Volume 032, No 27, 4/11/1930
New Mexico Lobo, Volume 032, No 27, 4/11 ...
University of New Mexico
core
ABSTRACT Arthrogryposis multiplex congenita (AMC) is a group of rare congenital conditions, characterized by multiple joint contractures but may involve any body system including central nervous system. AMC is etiologically heterogeneous, with over 400 genetic and many non‐genetic causes implicated in its prenatal development.
Shahrzad Nematollahi +20 more
wiley +1 more source
New Mexico Lobo, Volume 068, No 29, 11/4/1964
New Mexico Lobo, Volume 068, No 29, 11/4 ...
University of New Mexico
core
Withdrawal notice to Eruption of plaques, hemorrhagic bullae and vesicles
Sabah Osmani +3 more
doaj +1 more source

