听力与言语-语言病理学

行为科学

医学伦理学

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  • The use of enoxaparin in children with acute, nonhemorrhagic ischemic stroke.

    abstract::The use of low-molecular-weight heparin offers multiple advantages over unfractionated heparins in pediatric patients with acute ischemic stroke. The safety and efficacy of low-molecular-weight heparin have been demonstrated in adults, but less is known about their use in children. This study reviews retrospectively t...

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/s0887-8994(03)00270-4

    authors: Burak CR,Bowen MD,Barron TF

    更新日期:2003-10-01 00:00:00

  • Severe bilateral carpal tunnel syndrome in juvenile chronic arthritis.

    abstract::Carpal tunnel syndrome, although rare, is known to occur in children mainly because of genetic or metabolic disorders. The clinical findings are variable and include symptoms of burning pain, tingling, numbness, and weakness or atrophy in the hands of the patients. It is usually diagnosed by demonstration of prolonged...

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/s0887-8994(03)00280-7

    authors: Unal O,Ozçakar L,Cetin A,Kaymak B

    更新日期:2003-10-01 00:00:00

  • Fetal neurologic consultations.

    abstract::The pediatric neurologist can fulfill a useful role as a subspecialty consultant concerning the fetus with a suspected brain disorder, given that neurologic disease may occur before the intrapartum period. Brain disorders detected in the neonatal period may also reflect fetal brain damage before dysfunction is first d...

    journal_title:Pediatric neurology

    pub_type: 杂志文章,评审

    doi:10.1016/s0887-8994(03)00234-0

    authors: Scher MS

    更新日期:2003-09-01 00:00:00

  • Niemann-Pick type C disease associated with peripheral neuropathy.

    abstract::Niemann-Pick type C disease is an autosomal-recessive, inherited neurovisceral lipid storage disorder. This disease results from either protein NPC1 or HE1 deficiency, which leads to cholesterol metabolism disturbance and is characterized by early hepatosplenomegaly and progressive ataxia, dystonia, cataplexy, dysarth...

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/s0887-8994(03)00219-4

    authors: Zafeiriou DI,Triantafyllou P,Gombakis NP,Vargiami E,Tsantali C,Michelakaki E

    更新日期:2003-09-01 00:00:00

  • Rasmussen syndrome and long-term response to thalidomide.

    abstract::We report a 13-year-old female who experienced symptoms and signs of Rasmussen encephalitis for the first time at the age of 5 years. Various therapeutic procedures, including conventional and new antiepileptic drugs, steroids, immunoglobulin, plasma exchanges, and partial hemispherectomy, were applied, but their resu...

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/s0887-8994(03)00216-9

    authors: Marjanovic BD,Stojanov LM,Zdravkovic DS,Kravljanac RM,Djordjevic MS

    更新日期:2003-08-01 00:00:00

  • The diagnostic value of sensory evoked potentials in pediatric Wilson disease.

    abstract::We studied the sensory evoked potentials in pediatric Wilson disease to verify their subclinical neurologic involvement and to elucidate the role of cirrhosis in abnormal evoked potentials in non-neurologic Wilson disease. Thirty children (17 male, 13 female), diagnosed with Wilson disease before 18 years, were enroll...

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/s0887-8994(03)00026-2

    authors: Hsu YS,Chang YC,Lee WT,Ni YH,Hsu HY,Chang MH

    更新日期:2003-07-01 00:00:00

  • Onset of generalized seizures after intrathecal interferon therapy of SSPE.

    abstract::An 11-year-old male was admitted with inability to walk and speech abnormality. He was diagnosed with subacute sclerosing panencephalitis on the basis of clinical and laboratory findings. Therapy with inosiplex (100 mg/kg/day orally) plus intrathecal interferon-alpha (3 million units/dose twice per week) and ribavirin...

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/s0887-8994(03)00040-7

    authors: Caksen H,Odabaş D,Anlar O,Ataş B,Tuncer O

    更新日期:2003-07-01 00:00:00

  • A young infant with musicogenic epilepsy.

    abstract::Musicogenic epilepsy is a relatively rare form of epilepsy. In its pure form, it is characterized by epileptic seizures that are provoked exclusively by listening to music. The usual type of seizure is partial complex or generalized tonic-clonic. Precipitating factors are quite specific, such as listening to only one ...

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/s0887-8994(03)00011-0

    authors: Lin KL,Wang HS,Kao PF

    更新日期:2003-05-01 00:00:00

  • Uncoupling of EEG-clinical neonatal seizures after antiepileptic drug use.

    abstract::A prospective study of the efficacy of seizure cessation by phenobarbital versus phenytoin administration utilized both clinical and electroencephalographic expressions of seizure behaviors. The phenomenon of uncoupling was defined as the persistence of electrographic seizures despite the suppression of >or=50% clinic...

    journal_title:Pediatric neurology

    pub_type: 临床试验,杂志文章,随机对照试验

    doi:10.1016/s0887-8994(02)00621-5

    authors: Scher MS,Alvin J,Gaus L,Minnigh B,Painter MJ

    更新日期:2003-04-01 00:00:00

  • Oligohydrosis and fever in pediatric patients treated with zonisamide.

    abstract::Zonisamide is an antiepileptic drug developed and first marketed in Japan in 1989. Cases of oligohydrosis, characterized by deficient production and secretion of sweat, were reported in children treated with zonisamide in Japan during development and in the postmarketing period. Zonisamide was approved in the United S...

    journal_title:Pediatric neurology

    pub_type: 杂志文章,评审

    doi:10.1016/s0887-8994(02)00511-8

    authors: Knudsen JF,Thambi LR,Kapcala LP,Racoosin JA

    更新日期:2003-03-01 00:00:00

  • BH4-sensitive hyperphenylalaninemia: new case and review of literature.

    abstract::We report a patient with BH(4)-sensitive phenylketonuria. In neonatal screening, phenylalanine levels above 10 mg/dl were detected. In the tetrahydrobiopterin- (BH(4)) loading test, phenylalanine concentrations in serum fell significantly. Dihydropteridine reductase activity in blood, pterines, and neurotransmitters i...

    journal_title:Pediatric neurology

    pub_type: 杂志文章,评审

    doi:10.1016/s0887-8994(02)00516-7

    authors: Lücke T,Illsinger S,Aulehla-Scholz C,Sander J,Das AM

    更新日期:2003-03-01 00:00:00

  • Predicting neuropsychologic outcome after traumatic brain injury in children.

    abstract::The ability to predict long-term neurologic and neuropsychologic outcomes in 22 children, ages 1 week to 14 years at the time of traumatic brain injury, was investigated using proton magnetic resonance spectroscopy acquired post injury and compared with standardized neurologic, intellectual, and neuropsychologic testi...

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/s0887-8994(02)00491-5

    authors: Brenner T,Freier MC,Holshouser BA,Burley T,Ashwal S

    更新日期:2003-02-01 00:00:00

  • Transient nonketotic hyperglycinemia: two case reports and literature review.

    abstract::Transient nonketotic hyperglycinemia is characterized by clinical and biochemical findings similar to those seen in classic nonketotic hyperglycinemia. Abnormalities in amino acids are partially or completely resolved in a period ranging from days to months. Almost all patients with the classic form of nonketotic hype...

    journal_title:Pediatric neurology

    pub_type: 杂志文章,评审

    doi:10.1016/s0887-8994(02)00501-5

    authors: Aliefendioğlu D,Tana Aslan Ay,Coşkun T,Dursun A,Cakmak FN,Kesimer M

    更新日期:2003-02-01 00:00:00

  • Reduction of seizures with low-dose clonazepam in children with epilepsy.

    abstract::The acute effects of low-dose clonazepam on seizure frequency in children with epilepsy was evaluated. In an open study, 19 children with epilepsy (15 generalized and four partial) were examined during hospitalization with recordings of seizures by trained personnel. Seizures were counted during two 24-hour periods: b...

    journal_title:Pediatric neurology

    pub_type: 临床试验,杂志文章

    doi:10.1016/s0887-8994(02)00468-x

    authors: Dahlin MG,Amark PE,Nergårdh AR

    更新日期:2003-01-01 00:00:00

  • II. Perinatal brain tumors: a review of 250 cases.

    abstract::Central nervous system tumors occur considerably less often in the fetus and neonate than in the older child. They are not entirely the same as those present later in life. Their location, biologic behavior, response to therapy, and histologic types are different. Fetal and neonatal brain tumors (n = 250) were collect...

    journal_title:Pediatric neurology

    pub_type: 杂志文章,评审

    doi:10.1016/s0887-8994(02)00459-9

    authors: Isaacs H Jr

    更新日期:2002-11-01 00:00:00

  • Atypical MELAS associated with mitochondrial tRNA(Lys) gene A8296G mutation.

    abstract::We report on a unique patient with mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) presenting optic atrophy, cardiomyopathy, and bilateral striatal necrosis before stoke-like episodes became apparent. Skeletal muscle total mitochondrial DNA analysis identified a heteroplasmic ...

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/s0887-8994(02)00456-3

    authors: Sakuta R,Honzawa S,Murakami N,Goto Y,Nagai T

    更新日期:2002-11-01 00:00:00

  • Successful endovascular treatment of cerebral arteriovenous fistula.

    abstract::Childhood intracranial varix is rare and has been associated mostly with vein of Galen fistula or arteriovenous malformation. We present one patient with intracranial arteriovenous fistula with concomitant giant varix in a child. We treated the patient with endovascular embolization and obtained complete closure of fi...

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/s0887-8994(02)00424-1

    authors: Hung PC,Wang HS

    更新日期:2002-10-01 00:00:00

  • Update of the Amiel-Tison neurologic assessment for the term neonate or at 40 weeks corrected age.

    abstract::Amiel-Tison neurologic assessment at term has recently been updated for clinical application. Experience in this field, in addition to a better understanding of pathophysiologic characteristics of the immature brain, has taught us that an increased precision in assessing central nervous system function in the neonate ...

    journal_title:Pediatric neurology

    pub_type: 杂志文章,评审

    doi:10.1016/s0887-8994(02)00436-8

    authors: Amiel-Tison C

    更新日期:2002-09-01 00:00:00

  • Attitudes of medical students toward pediatric neurology.

    abstract::Planning strategies to encourage students to pursue a career in pediatric neurology requires assessment of their attitudes and career choices. A structured 30-item questionnaire was designed to examine students' attitudes toward pediatric neurology. In the study, 161 final-year medical students (1999-2000), 20-26 year...

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/s0887-8994(02)00386-7

    authors: Jan MM,Fida NM

    更新日期:2002-08-01 00:00:00

  • Vitamins ameliorate secondary mitochondrial failure in neonatal rat brain.

    abstract::Recirculation after transient intrauterine ischemia has previously been found to be accompanied by secondary mitochondrial dysfunction in the immature rat brain. This study was performed to assess the efficacy of combined treatment with ascorbic acid and alpha-tocopherol in improving secondary brain damage. On the 17t...

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/s0887-8994(02)00383-1

    authors: Nakai A,Shibazaki Y,Taniuchi Y,Oya A,Asakura H,Koshino T,Araki T

    更新日期:2002-07-01 00:00:00

  • An unusual manifestation of Wegener's granulomatosis in a 4-year-old girl.

    abstract::We report a female who was diagnosed with Wegener's granulomatosis at 4 years of age with life-threatening intracranial bleeding. The patient's serum was positive for c-antineutrophilic cytoplasmic antibodies, and histologic analysis of the lung biopsy revealed evidence of granulomatous vasculitis. Initial treatment w...

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/s0887-8994(02)00392-2

    authors: Haas JP,Metzler M,Ruder H,Waldherr R,Böswald M,Rupprecht T

    更新日期:2002-07-01 00:00:00

  • Congenital hypotonia with favorable outcome.

    abstract::Congenital hypotonia with favorable outcome is characterized by an early neonatal onset and a benign clinical course. The old term, proposed by Walton, was benign congenital hypotonia, denoting the presence of muscle weakness and hypotonia, with the exception of Werdnig-Hoffmann disease. It has been clear that this te...

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/s0887-8994(02)00379-x

    authors: Carboni P,Pisani F,Crescenzi A,Villani C

    更新日期:2002-05-01 00:00:00

  • Methotrexate leukoencephalopathy presenting as Klüver-Bucy syndrome and uncinate seizures.

    abstract::Methotrexate causes several biochemical changes that impact the nervous system. The neurotoxicity usually affects the cerebral white matter, causing a leukoencephalopathy that can be chronic and progressive with cognitive decline. A 15-year-old male developed olfactory seizures and behavioral abnormalities (hypersexua...

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/s0887-8994(01)00376-9

    authors: Antunes NL,Souweidane MM,Lis E,Rosenblum MK,Steinherz PG

    更新日期:2002-04-01 00:00:00

  • Hematogenous brain metastasis in children.

    abstract::Hematogenous brain metastases are uncommon in childhood. Three patients and a literature review that includes centers reporting up to 36 years of experience are presented in this study. The total of 2,040 patients includes our three examples of one neuroblastoma, one hepatoblastoma, and one adrenal carcinoma. Cerebral...

    journal_title:Pediatric neurology

    pub_type: 杂志文章,评审

    doi:10.1016/s0887-8994(01)00363-0

    authors: Curless RG,Toledano SR,Ragheb J,Cleveland WW,Falcone S

    更新日期:2002-03-01 00:00:00

  • Pediatric phantom vision (Charles Bonnet) syndrome.

    abstract::Visual symptomatology in childhood often presents diagnostic difficulties. Recurrent paroxysmal visual complaints, although typically associated with migraine, may also signal other disorders. We describe a 9-year-old partially sighted male with paroxysmal zoopsias resulting from Charles Bonnet syndrome. This conditio...

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/s0887-8994(01)00358-7

    authors: Mewasingh LD,Kornreich C,Christiaens F,Christophe C,Dan B

    更新日期:2002-02-01 00:00:00

  • Pediatric tumefactive demyelination: case series and review of the literature.

    abstract::Tumefactive demyelinating lesions may be misdiagnosed as brain neoplasms or abscesses. In this paper, we present four cases of pediatric tumefactive demyelination. Twelve cases of pediatric tumefactive demyelination previously reported in the English literature are also summarized. We describe the neuroimaging charact...

    journal_title:Pediatric neurology

    pub_type: 杂志文章,评审

    doi:10.1016/s0887-8994(01)00322-8

    authors: McAdam LC,Blaser SI,Banwell BL

    更新日期:2002-01-01 00:00:00

  • Central nervous system vasculopathy associated with neonatal lupus.

    abstract::Neonatal lupus erythematosus, characterized mainly by congenital heart block and transient skin lesions, is usually self-limited. A patient with history of neonatal lupus erythematosus and congenital heart block developed central nervous system vasculopathy resembling moyamoya disease and hypertension at 17 years of a...

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/s0887-8994(01)00344-7

    authors: Inoue K,Fukushige J,Ohno T,Igarashi H,Hara T

    更新日期:2002-01-01 00:00:00

  • Signal transduction for clinicians: why should we care?

    abstract::Neurons must respond to a bewildering array of external and internal stimuli and must distinguish among them to generate an appropriate response or change in metabolic or electrical activity. Furthermore, the response of a cell to a given stimulus must depend on what else is happening inside and outside the cell at th...

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/s0887-8994(01)00320-4

    authors: Schor NF

    更新日期:2001-11-01 00:00:00

  • Parry-Romberg syndrome associated with Adie's pupil and radiologic findings.

    abstract::We describe Adie's pupil and radiologic changes related to Parry-Romberg syndrome in a child who presented with facial hemiatrophy with no neurologic deficit. We suggest that cerebral lesions in Parry-Romberg syndrome without neurologic symptoms must be carefully investigated. ...

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/s0887-8994(01)00333-2

    authors: Aynaci FM,Sen Y,Erdöl H,Ahmetoğlu A,Elmas R

    更新日期:2001-11-01 00:00:00

  • Seizures associated with calcifications and edema in neurocysticercosis.

    abstract::We describe eight cases of pediatric patients whose neuroimages performed after seizures revealed abnormalities that were compatible with edema surrounding calcified lesions and which disappeared in subsequent examinations. ...

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/s0887-8994(01)00324-1

    authors: Antoniuk SA,Bruck I,Dos Santos LH,Pintarelli VL,Navolar FB,Brackmann PC Jr,de Morais RL

    更新日期:2001-10-01 00:00:00

  • Kawasaki disease with predominant central nervous system involvement.

    abstract::A 4-year-old female was hospitalized with clinical and electroencephalographic evidence of acute encephalopathy. Five days later the classic signs of Kawasaki disease appeared. The neurologic outcome in this female was poor despite early treatment with immunoglobulin. Like many other vasculitidies, Kawasaki disease ca...

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/s0887-8994(01)00290-9

    authors: Tabarki B,Mahdhaoui A,Selmi H,Yacoub M,Essoussi AS

    更新日期:2001-09-01 00:00:00

  • Hallervorden-Spatz syndrome.

    abstract::The historic and current status of Hallervorden-Spatz syndrome diagnosis, classification, and therapies are discussed. A number of symptomatic therapies are available and should be used optimally for each patient. Although one gene locus has been identified, many patients do not manifest linkage to the NBIA1 locus (ne...

    journal_title:Pediatric neurology

    pub_type: 杂志文章,评审

    doi:10.1016/s0887-8994(01)00253-3

    authors: Swaiman KF

    更新日期:2001-08-01 00:00:00

  • Mycoplasma pneumoniae infection, meningoencephalitis, and hemophagocytosis.

    abstract::Central nervous system manifestations are a common extrapulmonary complication of Mycoplasma pneumoniae infection, of which encephalitis is a well-recognized abnormality in children. In this report the first description of M. pneumoniae infection simultaneously complicated by meningoencephalitis and hemophagocytosis i...

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/s0887-8994(01)00274-0

    authors: Bruch LA,Jefferson RJ,Pike MG,Gould SJ,Squier W

    更新日期:2001-07-01 00:00:00

  • Clinical spectrum of reversible posterior leukoencephalopathy syndrome.

    abstract::Reversible posterior leukoencephalopathy syndrome is a recently recognized disorder with characteristic radiologic findings that mainly involve the white/gray matter of the parieto-occipital lobes. This complex syndrome is associated with cyclosporine A therapy or a variety of other conditions in which blood pressure ...

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/s0887-8994(01)00265-x

    authors: Kwon S,Koo J,Lee S

    更新日期:2001-05-01 00:00:00

  • Symptomatic or cryptogenic partial epilepsy of childhood onset: fourteen-year follow-up.

    abstract::This study reports on the seizure and psychosocial outcome of 29 patients with electroclinically well-defined childhood-onset symptomatogenic or cryptogenic partial epilepsy with complex partial seizures who were followed prospectively over 14 years. Many were refractory at the time of enrollment. At 14-year follow-up...

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/s0887-8994(01)00246-6

    authors: Szabó CA,Rothner AD,Kotagal P,Erenberg G,Dinner DS,Wyllie E

    更新日期:2001-04-01 00:00:00

  • Subclinical rhythmic EEG discharge of adults: SREDA in two children.

    abstract::Subclinical rhythmic electroencephalogram (EEG) discharge is an uncommon rhythmic EEG pattern that has been reported to occur in adults. It is thought to be a nonspecific finding with little clinical significance. This article reports this EEG pattern in two children and suggests it be called subclinical rhythmic EEG ...

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/s0887-8994(01)00238-7

    authors: Nagarajan L,Gregory PB,Hewitt IK,Gubbay SS,Parry TS

    更新日期:2001-04-01 00:00:00

  • Ocular motor dysfunction in Lesch-Nyhan disease.

    abstract::Eye movements were assessed in 22 patients with varying degrees of hypoxanthine-guanine phosphoribosyltransferase deficiency. Ocular motility was clinically normal in seven patients with moderate enzyme deficiency but grossly abnormal in 15 patients with severe enzyme deficiency. In patients with severe deficiency, fi...

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/s0887-8994(00)00265-4

    authors: Jinnah HA,Lewis RF,Visser JE,Eddey GE,Barabas G,Harris JC

    更新日期:2001-03-01 00:00:00

  • Cerebral vascular events associated with ulcerative colitis in children.

    abstract::Although peripheral vascular thrombic events are recognized as a serious extra-intestinal complication of inflammatory bowel disease, the occurrence of cerebral vascular events in association with acute exacerbations of this group of diseases is rare. In this article, relevant literature is reviewed and three children...

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/s0887-8994(00)00264-2

    authors: Keene DL,Matzinger MA,Jacob PJ,Humphreys P

    更新日期:2001-03-01 00:00:00

  • Recurrent intracranial ependymoma in children: salvage therapy with oral etoposide.

    abstract::Chronic oral VP-16 (etoposide) is a chemotherapy regimen with a wide application in oncology and documented efficacy against germ cell tumors, lymphomas, Kaposi's sarcoma, and primary brain tumors. This study was performed to assess the toxicity and activity of chronic oral etoposide in the management of children with...

    journal_title:Pediatric neurology

    pub_type: 临床试验,杂志文章

    doi:10.1016/s0887-8994(00)00249-6

    authors: Chamberlain MC

    更新日期:2001-02-01 00:00:00

  • Visual-evoked potentials in the assessment of optic gliomas.

    abstract::The most effective method for the screening and monitoring of optic pathway gliomas in children with neurofibromatosis type 1 remains a dilemma. Children less than 6 years of age are the group at highest risk for the development of optic pathway gliomas. Although an annual ophthalmologic examination currently is recom...

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/s0887-8994(00)00230-7

    authors: Ng YT,North KN

    更新日期:2001-01-01 00:00:00

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