Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Anthony A. Perszyk"'
Publikováno v:
Journal of Neurosurgery: Pediatrics. 16:186-194
OBJECT The cranium is documented to grow from birth through adolescence. The standard of practice in primary care is measuring head circumference and plotting growth using curves that stop at 36 months. The authors report the importance of their expe
Publikováno v:
American Journal of Perinatology. 20:025-032
A term male newborn, appropriate for gestational age, developed hypothermia, severe cardiac dysrrhythmia, and nonoliguric hyperkalemia within 24 hours of birth. Despite the prenatal identification of cystic renal dysplasia without oligohydramnios, at
Autor:
Anthony A. Perszyk, Bangalore R. Premachandra, Renu Sharma, Hongbo Li, Mark L. Hudak, Carmela Monteiro
Publikováno v:
American Journal of Perinatology. 17:201-206
A term infant with hydrops fetalis presented with hypotonia, massive splenomegaly, renal failure, and severe hyperferritinemia. Multiple organ failure, myoclonus, and opisthotonus ensued and she died at 15 days of age. High rounded forehead, large op
Autor:
Hector E. James, Anthony A. Perszyk
Publikováno v:
Pediatric neurosurgery. 47(5)
Purpose: Infants and children with microcrania are referred to pediatric neurosurgeons for evaluation and treatment of possible craniosynostosis and other disorders. We present an approach to these children to facilitate the appropriate clinical eval
Autor:
C Aslan Beyza, Anthony A. Perszyk
Publikováno v:
Mitochondrion. 24:S19
Multiple acyl-CoA dehydrogenation deficiency (MADD), or commonly referred to as glutaric acidemia type 2 (GA2), is a genetic metabolic disorder affecting amino acid, fatty acid, and choline mechanisms. It is passed on in an autosomal-recessive manner
Publikováno v:
Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society. 2(1)
Disorders associated with mitochondrial DNA (mtDNA) mutations are usually dominated by involvement of the nervous system and skeletal muscle (hence the term “mitochondrial encephalomyopathies”). However, considering the high dependence of the hea