听力与言语-语言病理学

行为科学

医学伦理学

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  • Febrile seizures--treatment and outcome.

    abstract::Assessment of treatment strategies in febrile seizures should be based on short- and long-term outcomes, with and without acute, intermittent, or chronic medical intervention, as well as short- and long-term side effects. Febrile seizures are a benign condition with a normal neurological, motor, intellectual, and cogn...

    journal_title:Brain & development

    pub_type: 杂志文章,评审

    doi:10.1016/s0387-7604(96)00059-9

    authors: Knudsen FU

    更新日期:1996-11-01 00:00:00

  • Nerve growth factor and the neurotrophic factor hypothesis.

    abstract::The discovery of nerve growth factor (NGF) over 40 years ago led to the formulation of the "Neurotrophic Factor Hypothesis". This hypothesis states that developing neurons compete with each other for a limited supply of a neurotrophic factor (NTF) provided by the target tissue. Successful competitors survive; unsucces...

    journal_title:Brain & development

    pub_type: 杂志文章,评审

    doi:10.1016/0387-7604(96)00051-4

    authors: Yuen EC,Howe CL,Li Y,Holtzman DM,Mobley WC

    更新日期:1996-09-01 00:00:00

  • Infantile myositis presenting in the neonatal period.

    abstract::Infantile myositis, observed in the neonatal period, is rare and may be confused with congenital muscular dystrophy. The patient presented here showed evidence of a myopathy with in utero onset with intrauterine growth retardation and decreased fetal movements. A muscle biopsy demonstrated characteristic perifascicula...

    journal_title:Brain & development

    pub_type: 杂志文章

    doi:10.1016/0387-7604(96)00049-6

    authors: Vajsar J,Jay V,Babyn P

    更新日期:1996-09-01 00:00:00

  • Sensorineural deafness in siblings with adenosine deaminase deficiency.

    abstract::Two siblings with adenosine deaminase deficiency were successfully treated with allogeneic bone marrow transplantation without conditioning. Although the patients were free from infections after immunologic reconstitution, both showed sensorineural deafness at 1 year of age. Because there were no structural abnormalit...

    journal_title:Brain & development

    pub_type: 杂志文章

    doi:10.1016/0387-7604(96)00014-9

    authors: Tanaka C,Hara T,Suzaki I,Maegaki Y,Takeshita K

    更新日期:1996-07-01 00:00:00

  • Correlation between CSWS and aphasia in Landau-Kleffner syndrome: a study of three cases.

    abstract::We report three typical cases of Landau-Kleffner syndrome with varied courses. The very frequent discharges in sleep EEGs, often showing the patterns of CSWS (continuous spike-waves during slow-wave sleep), either typical (spike-wave complex occupying over 85% of slow-wave sleep duration) or atypical (spike-waves occu...

    journal_title:Brain & development

    pub_type: 杂志文章

    doi:10.1016/0387-7604(95)00168-9

    authors: Li M,Hao XY,Qing J,Wu XR

    更新日期:1996-05-01 00:00:00

  • A case of infantile spasms: epileptic apnea as partial seizures at onset.

    abstract::We report a 2-month-old boy who presented with apneic attacks as a manifestation of epileptic seizures at onset and eventually progressed to infantile spasms. At onset, at 2 months of age, apneic attacks were the sole symptom of epileptic fits. Although these seizures were accompanied by cyanosis, bradycardia was not ...

    journal_title:Brain & development

    pub_type: 杂志文章

    doi:10.1016/0387-7604(95)00148-4

    authors: Kamei A,Ichinohe S,Ito M,Fujiwara T

    更新日期:1996-05-01 00:00:00

  • Vasopressin in the cerebrospinal fluid of febrile children with or without seizures.

    abstract::Immaturity in water and electrolyte balance in the brain has been considered to increase the susceptibility of young animals and children to febrile convulsions (FCs). Arginine-vasopressin (AVP) is involved in the regulation of several centrally mediated events such as modulation of fever and the ease with which water...

    journal_title:Brain & development

    pub_type: 临床试验,杂志文章

    doi:10.1016/0387-7604(95)00146-8

    authors: Kiviranta T,Tuomisto L,Jolkkonen J,Airaksinen EM

    更新日期:1996-03-01 00:00:00

  • Diffuse white matter lesions associated with herpes simplex encephalitis as observed on magnetic resonance imaging.

    abstract::A 2-year-old boy with herpes simplex encephalitis developed diffuse brain lesions involving the white matter of both cerebral hemispheres. These lesions in the white matter were clearly observed on magnetic resonance imaging (MRI) with the T2-weighted sequence, and were found to have spontaneously disappeared on subse...

    journal_title:Brain & development

    pub_type: 杂志文章

    doi:10.1016/0387-7604(95)00141-7

    authors: Tamura T,Morikawa A,Kikuchi K

    更新日期:1996-03-01 00:00:00

  • Morphometric development of the human fetal auditory system: inferior collicular nucleus.

    abstract::The development of the human inferior collicular nucleus was studied on serial sections of the brains of 9 fetuses at 12-34 weeks of gestation and an adult of 63 years using an electronic planimeter with a computer. Morphometric analysis of the development of the inferior collicular nucleus showed that its development...

    journal_title:Brain & development

    pub_type: 杂志文章

    doi:10.1016/0387-7604(95)00089-5

    authors: Nara T,Goto N,Hamano S,Okada A

    更新日期:1996-01-01 00:00:00

  • Arteriovenous malformation in hypomelanosis of Ito.

    abstract::Hypomelanosis of Ito (HI) is a neurocutaneous syndrome with multisystemic involvement. Its most frequent neurological abnormalities are mental retardation and seizures. EEG, CT and MRI findings are not characteristic enough to be diagnostic. In this report, we describe a patient with typical cutaneous lesions of HI an...

    journal_title:Brain & development

    pub_type: 杂志文章

    doi:10.1016/0387-7604(95)00101-8

    authors: Urgelles E,Pascual-Castroviejo I,Roche C,Moneo JL,Martinez MA,Vega A

    更新日期:1996-01-01 00:00:00

  • Posterior fossa cystic lesions--magnetic resonance imaging manifestations.

    abstract::Cystic lesions of the posterior fossa remain a controversial subject as to clinical classification and diagnosis, especially for those in combination with other intracranial abnormalities. During the period of November 1985 to June 1991, 16 patients with cystic lesions of the posterior fossa were retrospectively revie...

    journal_title:Brain & development

    pub_type: 杂志文章

    doi:10.1016/0387-7604(95)00067-4

    authors: Tan EC,Takagi T,Karasawa K

    更新日期:1995-11-01 00:00:00

  • Benign convulsions with mild gastroenteritis: a report of 10 recent cases detailing clinical varieties.

    abstract::To better define the characteristic clinical features of benign convulsions with mild gastroenteritis, recently recognized as a new entity in Japan, we reviewed all the 10 patients we have seen from 1992 to 1994. The clinical features have been previously reported in the literature to be afebrile generalized tonic-clo...

    journal_title:Brain & development

    pub_type: 杂志文章

    doi:10.1016/0387-7604(95)00074-l

    authors: Komori H,Wada M,Eto M,Oki H,Aida K,Fujimoto T

    更新日期:1995-09-01 00:00:00

  • Congenital muscular dystrophy with eye and brain involvement. The Turkish experience in two cases.

    abstract::Eye and brain involvement in congenital muscular dystrophies (CMD) constitute a distinct group with a spectrum of brain malformations. We report two such CMD patients among our series of 58 cases with CMD. Despite known clinical and neuroradiological overlap, we tend to classify them into specific syndromes, though th...

    journal_title:Brain & development

    pub_type: 杂志文章

    doi:10.1016/0387-7604(95)00047-f

    authors: Topaloğlu H,Cila A,Taşdemir AH,Saatçi I

    更新日期:1995-07-01 00:00:00

  • Basal encephaloceles with morning glory syndrome, and progressive hormonal and visual disturbances: case report and review of the literature.

    abstract::We report an 11-year-old girl with progressive hypopituitarism and visual loss of the right eye caused by trans-sphenoidal and sphenoethmoidal encephaloceles associated with morning glory syndrome. She was first seen at the age of 8 years, because of polydipsia and polyuria, and examination at that time revealed pitui...

    journal_title:Brain & development

    pub_type: 杂志文章,评审

    doi:10.1016/0387-7604(95)00021-3

    authors: Morioka M,Marubayashi T,Masumitsu T,Miura M,Ushio Y

    更新日期:1995-05-01 00:00:00

  • Clinical and MRI findings in a case of D-2-hydroxyglutaric aciduria.

    abstract::We report the 3rd case in the literature of a 3-year-old boy with D-2-hydroxyglutaric (D-2-HG) aciduria, who presented primarily generalized hypotonia and feeding difficulty during the neonatal period, with eventual development of generalized myoclonic seizures. Gas chromatographic analysis of urinary organic acids sh...

    journal_title:Brain & development

    pub_type: 杂志文章,评审

    doi:10.1016/0387-7604(94)00123-f

    authors: Sugita K,Kakinuma H,Okajima Y,Ogawa A,Watanabe H,Niimi H

    更新日期:1995-03-01 00:00:00

  • Abnormality of cerebral gangliosides in Fukuyama type congenital muscular dystrophy.

    abstract::Compared with DMD cases and non-neuromuscular disease controls, FCMD cases showed a reduction of total gangliosides, and an abnormal, immature ganglioside pattern in the cerebral gray and white matter. However, GM4, which is only found in myelin and oligodendroglia, and is a unique quantitative marker of myelination, ...

    journal_title:Brain & development

    pub_type: 杂志文章

    doi:10.1016/0387-7604(94)00114-d

    authors: Izumi T,Hara K,Ogawa T,Osawa M,Saito K,Novo ML,Fukuyama Y,Takashima S

    更新日期:1995-01-01 00:00:00

  • Deflazacort vs. prednisone in Duchenne muscular dystrophy: trends of an ongoing study.

    abstract::Several studies have demonstrated the slowing effect of corticosteroids on the decline of muscle strength in Duchenne muscular dystrophy (DMD). Deflazacort (DFC) is supposed to have fewer side effects than prednisone (PRED). An ongoing double blind multicenter study is comparing the effects and side effects of deflaza...

    journal_title:Brain & development

    pub_type: 临床试验,杂志文章,多中心研究

    doi:

    authors: Reitter B

    更新日期:1995-01-01 00:00:00

  • 3-Ketothiolase deficiency: a review and four new patients with neurologic symptoms.

    abstract::3-Ketothiolase deficiency (3KTD) manifests with intermittent acidosis and is due to deficiency of mitochondrial 2-methylacetoacetate thiolase. Only 22 patients have been previously reported. Although its variable clinical presentation is recognized, the associated neurological findings have not been detailed. We repor...

    journal_title:Brain & development

    pub_type: 杂志文章

    doi:10.1016/0387-7604(94)90095-7

    authors: Ozand PT,Rashed M,Gascon GG,al Odaib A,Shums A,Nester M,Brismar J

    更新日期:1994-11-01 00:00:00

  • Urinary N-acetyl-beta-glucosaminidase and guanidinoacetic acid levels in epileptic patients treated with anti-epileptic drugs.

    abstract::We investigated potential renal functional impairment induced by chronic use of anti-epileptic drugs (AEDs) in 79 epileptic children. They were divided into five groups: valproic acid (VPA) monotherapy where the serum concentration (SC) of VPA was no less than 60 micrograms/ml (VPA [SC > or = 60]) (15 cases), VPA mono...

    journal_title:Brain & development

    pub_type: 杂志文章

    doi:10.1016/0387-7604(94)90003-5

    authors: Otsuka T,Sunaga Y,Hikima A

    更新日期:1994-11-01 00:00:00

  • Pathological and biochemical studies of fetal Krabbe disease.

    abstract::Morphological and biochemical analysis of tissue from a 21-week-old fetus with Krabbe disease was performed. Galactosylceramidase activity was virtually absent in cultured amniotic cells obtained during the pregnancy of this fetus. The prenatal diagnosis was confirmed by enzymatic analysis of fetal cultured skin fibro...

    journal_title:Brain & development

    pub_type: 杂志文章

    doi:10.1016/0387-7604(94)90013-2

    authors: Ida H,Rennert OM,Watabe K,Eto Y,Maekawa K

    更新日期:1994-11-01 00:00:00

  • Cerebellar primary germ-cell tumor in a young boy.

    abstract::Germ cell tumors originating in the posterior fossa are very rare. Described herein is a case of primary germ cell tumor (yolk sac tumor) found in the cerebellar vermis. A 5-year-old boy who complained of headache was admitted. CT and MRI revealed a tumor with diffuse enhancement by contrast medium in the right cerebe...

    journal_title:Brain & development

    pub_type: 杂志文章

    doi:10.1016/0387-7604(94)90128-7

    authors: Nakase H,Ohnishi H,Touho H,Karasawa J,Tsunoda S

    更新日期:1994-09-01 00:00:00

  • Short latency somatosensory evoked potentials and 99mTc-HMPAO SPECT in a case of flunarizine-effective alternating hemiplegia in infancy.

    abstract::Short latency somatosensory evoked potentials (SSEPs) and 99mTc-hexamethylpropylene amine oxime single photon emission computed tomography (99mTc-HMPAO SPECT) were examined in a patient with alternating hemiplegia in infancy (AHI) before and after flunarizine treatment. The low amplitude and elongation of the latency ...

    journal_title:Brain & development

    pub_type: 杂志文章

    doi:10.1016/0387-7604(94)90032-9

    authors: Imamura A,Komori Y,Fukutomi O,Shimozawa N,Suzuki Y,Kondo N,Orii T

    更新日期:1994-07-01 00:00:00

  • Brain tumors and anorexia nervosa syndrome.

    abstract::This review presents 21 cases, found in the literature, of a CNS lesion (a tumor in 19 of them) associated with emaciation, anorexia and several psychic symptoms that had led to the diagnosis of anorexia nervosa (AN). Anorexia and psychic disturbances preceded the neurologic signs and/or the correct diagnosis in all p...

    journal_title:Brain & development

    pub_type: 杂志文章,评审

    doi:10.1016/0387-7604(94)90064-7

    authors: Chipkevitch E

    更新日期:1994-05-01 00:00:00

  • A case of cerebral aneurysm associated with complex partial seizures.

    abstract::We report a 20-month-old girl with an unruptured aneurysm of the middle cerebral artery. The initial sign was complex partial seizures. Magnetic resonance angiography showed an aneurysm of the right middle cerebral artery. Cerebral angiography confirmed the presence of a saccular aneurysm. After 3 months, the aneurysm...

    journal_title:Brain & development

    pub_type: 杂志文章

    doi:10.1016/0387-7604(94)90076-0

    authors: Tanaka K,Hirayama K,Hattori H,Matsuoka O,Sakamoto H,Hakuba A,Murata R

    更新日期:1994-05-01 00:00:00

  • Hereditary progressive dystonia with marked diurnal fluctuation (Segawa syndrome) in Taiwan.

    abstract::Since 1988, we have diagnosed 6 cases of hereditary progressive dystonia with marked diurnal fluctuation (HPD) in Taiwan. All cases presented with clinical features similar to those described by Segawa. They consisted of four sporadic and two familial cases. The age at onset ranged from 18 months to 8 years. There is ...

    journal_title:Brain & development

    pub_type: 杂志文章

    doi:10.1016/0387-7604(94)90048-5

    authors: Wang PJ,Ko YM,Young C,Hwu WL,Shen YZ

    更新日期:1994-03-01 00:00:00

  • Enteral formula feeds interfere with phenytoin absorption.

    abstract::Two children treated for status epilepticus had low plasma phenytoin levels during enteral feeding, despite adequate oral dosage. The target range (10-20 mg/l) was achieved when feeds were stopped, or when intravenous phenytoin was used. Enteral feeding may interfere with the absorption of oral phenytoin thereby compr...

    journal_title:Brain & development

    pub_type: 杂志文章

    doi:10.1016/0387-7604(94)90058-2

    authors: O'Hagan M,Wallace SJ

    更新日期:1994-03-01 00:00:00

  • A case of neonatal spinal cord injury: magnetic resonance imaging and somatosensory evoked potentials.

    abstract::This is the first case report on the diagnosis of spinal cord injury due to hemorrhage during the neonatal period using magnetic resonance imaging (MRI). Somatosensory evoked potentials are also helpful in the functional demonstration of this lesion. When discrepant signs, alert consciousness and intact cranial nerves...

    journal_title:Brain & development

    pub_type: 杂志文章

    doi:10.1016/0387-7604(94)90114-7

    authors: Minami T,Ise K,Kukita J,Koyanagi T,Ueda K

    更新日期:1994-01-01 00:00:00

  • A case of chronic epileptic encephalopathy of neonatal onset. A probable concern of human cytomegalovirus.

    abstract::A 10-year-old male patient, who had suffered from intractable convulsions from the neonatal period, is presented. Serial brain images suggested slow, gradual destruction of neural elements. Human cytomegalovirus (HCMV) DNA was detected in his cerebrospinal fluid (CSF) by means of the polymerase chain reaction. Intrath...

    journal_title:Brain & development

    pub_type: 杂志文章

    doi:10.1016/0387-7604(93)90086-n

    authors: Kohyama J,Suzuki N,Kajiwara M,Shimohira M,Iwakawa Y

    更新日期:1993-11-01 00:00:00

  • Recent advances in non-invasive studies of higher brain functions.

    abstract::Recent advances in modern technologies have enabled us to investigate higher brain functions non-invasively in human subjects. These techniques include topographic analysis of the scalp-recorded electric potentials, recording of the magnetic field generated from the brain, measurement of regional cerebral blood flow c...

    journal_title:Brain & development

    pub_type: 杂志文章,评审

    doi:10.1016/0387-7604(93)90081-i

    authors: Shibasaki H

    更新日期:1993-11-01 00:00:00

  • High doses of penicillin decreases [3H]flunitrazepam binding sites in rat neuron primary culture.

    abstract::Penicillin (PC) neurotoxicity (convulsions and encephalopathy) is considered to be due to GABAergic inhibition. The effects of penicillin G(PCG) on [3H]flunitrazepam (FNZ) binding in rat neuron-enriched primary cultures was examined to assess the role of the benzodiazepine (BDZ) receptor in the neurotoxicity. PCG appl...

    journal_title:Brain & development

    pub_type: 杂志文章

    doi:10.1016/0387-7604(93)90121-n

    authors: Shiraishi H,Ito M,Go T,Mikawa H

    更新日期:1993-09-01 00:00:00

  • Sequential MRI findings in a patient with a germ cell tumor in the basal ganglia.

    abstract::Serial changes of MRI scanning of an 11-year-old boy with hemiparesis due to a germ cell tumor in the basal ganglia are presented. Initial brain MRI T1-weighted images revealed a subtle mixed signal intensity lesion at left anterior and posterior limbs of the internal capsule. This lesion was not enhanced with Gd-DTPA...

    journal_title:Brain & development

    pub_type: 杂志文章

    doi:10.1016/0387-7604(93)90024-3

    authors: Takano T,Matsui E,Yamano T,Shimada M,Nakasu Y,Handa J

    更新日期:1993-07-01 00:00:00

  • Learning disorders and delinquency.

    abstract::Learning disorders of various types are relatively common, and the reaction of the affected child can lead to social problems. The higher the children's intelligence the more frustrated they can become. Lack of self-esteem can cause unacceptable behaviour in trying to counteract this, and boost the child's confidence....

    journal_title:Brain & development

    pub_type: 杂志文章,评审

    doi:10.1016/0387-7604(93)90060-l

    authors: Gordon N

    更新日期:1993-05-01 00:00:00

  • Electroencephalographic features of epileptic drop attacks and absence seizures: a case study.

    abstract::A study of epileptic drop attacks (EDA) by simultaneous video-polygraphic recordings was carried out in one epileptic patient with myoclonic astatic seizures (Doose syndrome). EDA was shown to correspond to a burst of generalized bilaterally synchronous spike and wave complexes (GBSSW) at 3 Hz. Absence seizures were a...

    journal_title:Brain & development

    pub_type: 杂志文章

    doi:10.1016/0387-7604(93)90070-o

    authors: Oguni H,Imaizumi Y,Uehara T,Oguni M,Fukuyama Y

    更新日期:1993-05-01 00:00:00

  • Two siblings with partial trisomy 1(q42.3-ter).

    abstract::Two brothers, aged 6 and 4 years, with an unbalanced chromosome translocation (partial trisomy 1), and their mother, a balanced carrier of the translocation, t(1;3)(q42.3;p26.3), were described. Both patients show minor anomalies; a large head with a prominent forehead, low-set and soaring ears, a high-arched palate, ...

    journal_title:Brain & development

    pub_type: 杂志文章

    doi:10.1016/0387-7604(93)90048-d

    authors: Sunaga Y,Ohtsuka T,Nagashima K,Kuroume T

    更新日期:1993-03-01 00:00:00

  • Immunological aspects of epilepsy.

    abstract::Approximately 10% of patients with systemic lupus erythematosus (SLE) develop epileptic seizures. When occurring before the onset of generalized SLE, the seizures are mainly primary generalized. Accordingly, long-term treatment with anti-epileptic drugs may precipitate SLE, or epilepsy and SLE may both occur as manife...

    journal_title:Brain & development

    pub_type: 杂志文章,评审

    doi:10.1016/0387-7604(93)90005-s

    authors: Aarli JA

    更新日期:1993-01-01 00:00:00

  • Stroke in neonates with cardiac right-to-left shunt.

    abstract::Neonatal focal cerebral arterial infarction has been rarely reported in the literature, in contrast to the watershed infarctions, which are common entities among asphyxiated infants. In neonatal postmortem series, thromboembolism was the commonest cause of cerebral arterial occlusion; the source of emboli was associat...

    journal_title:Brain & development

    pub_type: 杂志文章

    doi:10.1016/s0387-7604(12)80344-5

    authors: Pellicer A,Cabañas F,García-Alix A,Pérez-Higueras A,Quero J

    更新日期:1992-11-01 00:00:00

  • Early infantile epileptic encephalopathy: a case associated with hemimegalencephaly.

    abstract::The authors report a case of early infantile epileptic encephalopathy (EIEE) associated with hemimegalencephaly. The etiological factors in previously published cases of EIEE are reviewed and attention is focused on the high proportion of cases associated with neuronal migration disorders. We suggest that idiopathic c...

    journal_title:Brain & development

    pub_type: 杂志文章,评审

    doi:10.1016/s0387-7604(12)80356-1

    authors: Bermejo AM,Martin VL,Arcas J,Perez-Higueras A,Morales C,Pascual-Castroviejo I

    更新日期:1992-11-01 00:00:00

  • Alternating hemiplegia in childhood: 23 cases in Japan.

    abstract::Alternating hemiplegia in childhood (AHC) has clinically characteristic features which are easily defined and recognizable. Laboratory investigations were basically normal although they were extensively examined during and between attacks. There is still much debate about its etiology, particularly its relation to mig...

    journal_title:Brain & development

    pub_type: 杂志文章,评审

    doi:10.1016/s0387-7604(12)80144-6

    authors: Sakuragawa N

    更新日期:1992-09-01 00:00:00

  • Clinical variation within sibships in Fukuyama-type congenital muscular dystrophy.

    abstract::A family in which three siblings were affected with severe cerebral malformations in association with ocular anomalies and muscle disease is reported. One sibling was diagnosed as having Fukuyama type congenital muscular dystrophy (FCMD) because he showed severe hypotonia with dystrophic findings on a muscle biopsy in...

    journal_title:Brain & development

    pub_type: 杂志文章

    doi:10.1016/s0387-7604(12)80154-9

    authors: Yoshioka M,Kuroki S,Nigami H,Kawai T,Nakamura H

    更新日期:1992-09-01 00:00:00

  • Serum creatine-kinase-BB concentration in very low birth weight babies with posthemorrhagic ventricular dilatation.

    abstract::The association between measurements of lateral ventricle dilatation determined by serial ultrasound and brain specific creatine-kinase isoenzyme patterns (CK-BB) is studied in 60 very low birth weight preterm neonates of 1,500 g birth weight or 32 weeks gestation or less. The patients were divided into three groups a...

    journal_title:Brain & development

    pub_type: 杂志文章

    doi:10.1016/s0387-7604(12)80234-8

    authors: Amato M,Hüppi P,Gambon R

    更新日期:1992-07-01 00:00:00

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