Zobrazeno 1 - 10
of 53
pro vyhledávání: '"Pen-Jung Wang"'
Autor:
Pen Jung Wang, Kun Ruey Shieh, Terry B.J. Kuo, Yue-Loong Hsin, Cheryl C.H. Yang, Tomor Harnod
Publikováno v:
Seizure. 17:297-301
Summary Objective Repetitive seizures can alter the regulation of cardiac activity by the autonomic nervous system (ANS), and ANS dysregulation is thought to be associated with higher morbidity and mortality in epileptic patients, especially from sud
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8d481eb9b2ef8d20b2a9564ad147b408
https://doi.org/10.1016/j.seizure.2007.09.002
https://doi.org/10.1016/j.seizure.2007.09.002
Publikováno v:
Brain and Development. 27:101-107
Prader-Willi syndrome (PWS) and Angelman syndrome (AS) are two clinically distinct neurobehavioral syndromes that are caused by deficiency of gene expression from paternally or maternally derived homologues on chromosome 15q11-q13, respectively. Clin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9460a445da1dbd33845a32f641e816a6
https://doi.org/10.1016/j.braindev.2003.11.009
https://doi.org/10.1016/j.braindev.2003.11.009
Publikováno v:
The Pediatric Infectious Disease Journal. 23:671-674
Human herpesvirus 8 has been implicated in the pathogenesis of a limited subset of lymphoproliferative disorders in adults, but its role in children is unclear. A prospective evaluation of children with atypical lymphocytosis residing in the Hualien
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::99f1246aebab15b337ee4fed989a9987
https://doi.org/10.1097/01.inf.0000128776.45784.80
https://doi.org/10.1097/01.inf.0000128776.45784.80
Autor:
Yi-Hung Chou, Pen-Jung Wang
Publikováno v:
Journal of Child Neurology. 17:510-514
To evaluate the effect of early treatment of congenital hypothyroidism on central nervous system development, auditory brainstem evoked potentials were determined in 32 patients with hyperthyrotropinemia diagnosed during neonatal screening. The patie
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1ca0b366c9266df818f426981879c15f
https://doi.org/10.1177/088307380201700707
https://doi.org/10.1177/088307380201700707
Publikováno v:
Journal of Clinical Neurophysiology. 18:25-32
The purpose of this study is to explore and compare epileptic seizures and EEG evolution in the various types of genetic leukodystrophy (GL). The authors reviewed the medical records and analyzed 69 serial EEGs in 27 patients with GLs: 13 with late i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e3ce938f8cab3d31669cd0b2ddff4297
https://doi.org/10.1097/00004691-200101000-00006
https://doi.org/10.1097/00004691-200101000-00006
Publikováno v:
Pediatric Neurology. 20:295-300
Two infants with the neonatal type of nonketotic hyperglycinemia that had manifested as early neonatal consciousness disturbance are presented. Transient hyperammonemia had been detected in both initially. High levels of glycine in plasma and cerebro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0e9977f3f8abf08dc7a96f360a7a2dbc
https://doi.org/10.1016/s0887-8994(98)00157-x
https://doi.org/10.1016/s0887-8994(98)00157-x
Publikováno v:
Brain and Development. 20:530-535
To re-evaluate the diagnostic criteria for early myoclonic encephalopathy (EME), the following study was done. During the past 2 years, five patients with erratic, fragmentary myoclonus of neonatal onset, in association with other types of seizures,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7f198d3b4100072e0b4c90844e6920ea
https://doi.org/10.1016/s0387-7604(98)00042-4
https://doi.org/10.1016/s0387-7604(98)00042-4
Publikováno v:
Pediatric Neurology. 19:230-233
The human tail is a congenital anomaly with a protruding lesion from the lumbosacrococcygeal region. A newborn with a tail-like structure over the coccygeal area observed since birth is presented. Lipoma accompanied by tethered spinal cord were found
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c533ea5293e435ca9f3c64b319904cef
https://doi.org/10.1016/s0887-8994(98)00046-0
https://doi.org/10.1016/s0887-8994(98)00046-0
Publikováno v:
Clinical Neurology and Neurosurgery. 99:S118-S122
From January 1990 to December 1995, a total of nine cases of Moyamoya disease were treated at the National Taiwan University Hospital with combined encephalo-arterio-synangiosis (EAS) and encephalo-myo-synangiosis (EMS). There were five males and fou
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5ab07cc4ac4e20cddef4e4229631388b
https://doi.org/10.1016/s0303-8467(97)00070-x
https://doi.org/10.1016/s0303-8467(97)00070-x
Publikováno v:
Pediatric Neurology. 16:17-22
Angelman syndrome (AS) is characterized by severe psychomotor retardation, speech impairment, happy disposition with bursts of laughter, ataxia, convulsions, and some distinct physical anomalies. Correct diagnosis of AS is important because of its cl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::00ec61eda15f10f6526de25b54a98d86
https://doi.org/10.1016/s0887-8994(96)00264-0
https://doi.org/10.1016/s0887-8994(96)00264-0