The treatment of acute polyradiculoneuritis with respiratory paralysis.

Abstract:

:This paper reports 504 cases admitted with acute polyradiculoneuritis (AP) to Beijing Children's Hospital from 1975 through 1984. 343 of the 504 cases (68.1%) with AP had respiratory paralysis and in 198/504 (39.3%), tracheotomy was performed. In this study, none of the patients received steroids. We attempted to assess the grades of respiratory paralysis and established the criteria for tracheotomy. We also must perform the following procedures: 1) Artificial ventilation must be used correctly, 2) The secretion should be aspirated regularly in order to maintain a clear airway, 3) Sterilization must be strictly conducted to prevent cross infection. As a result, of 504 cases with AP 9 died, the mortality rate being 1.79%. The study suggests tracheotomy should be performed early and it is one of the most important procedures in the treatment of AP with respiratory paralysis.

journal_name

Brain Dev

journal_title

Brain & development

authors

Wu HS,Yei QF,Liu TC,Zhang WC

subject

Has Abstract

pub_date

1988-01-01 00:00:00

pages

147-9

issue

3

eissn

0387-7604

issn

1872-7131

pii

S0387-7604(88)80017-2

journal_volume

10

pub_type

杂志文章
  • Sensory hypersensitivity in Tourette syndrome: A review.

    abstract::Tourette syndrome (TS) is a neurodevelopmental disorder defined by tics, but most patients also experience bothersome sensory phenomena, in the form of premonitory urges and/or sensory hypersensitivity. Whereas premonitory urges are temporally paired with tics, sensory hypersensitivity is a constant, heightened awaren...

    journal_title:Brain & development

    pub_type: 杂志文章,评审

    doi:10.1016/j.braindev.2020.06.003

    authors: Isaacs D,Riordan H

    更新日期:2020-10-01 00:00:00

  • The association of epileptic focus estimated by magnetoencephalography with cognitive function in non-lesional epilepsy with continuous spikes and waves during slow wave sleep (ECSWS) children.

    abstract:OBJECTIVE:Epilepsy with continuous spikes and waves during slow sleep (ECSWS) is associated with cognitive deficits. The underlying mechanism is thought to relate to disturbance of functions of the foci by the persistent epileptic activity. However, the relationship between epileptic foci and cognitive deficits remains...

    journal_title:Brain & development

    pub_type: 杂志文章

    doi:10.1016/j.braindev.2018.09.005

    authors: Magara S,Komatsubara T,Hojo M,Kobayashi Y,Yoshino M,Saitoh A,Tohyama J

    更新日期:2019-02-01 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

  • 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

  • Aquaporin-4 autoimmunity in a child without optic neuritis and myelitis.

    abstract::Neuromyelitis optica (NMO) is an inflammatory demyelinating disease with a poor prognosis that is characterized by inflammatory optic neuritis and myelitis. Although it is commonly misdiagnosed as multiple sclerosis (MS), distinguishing NMO from MS is important, as therapeutic approaches approved for MS are ineffectiv...

    journal_title:Brain & development

    pub_type: 杂志文章

    doi:10.1016/j.braindev.2014.03.015

    authors: Numata Y,Uematsu M,Suzuki S,Miyabayashi T,Oyama T,Kubota S,Itoh T,Hino-Fukuyo N,Takahashi T,Kure S

    更新日期:2015-01-01 00:00:00

  • Influence of ACTH therapy on overnight sleep polygrams in infantile spasms.

    abstract::Overnight sleep polygrams were recorded before and during therapy in nine patients with infantile spasms. Results showed that ACTH therapy increased the waking time and decreased rapid eye movement sleep. Thus it caused sleep disturbance in patients with infantile spasms. During ACTH therapy the number of rapid eye mo...

    journal_title:Brain & development

    pub_type: 杂志文章

    doi:10.1016/s0387-7604(81)80006-x

    authors: Hashimoto T,Hiura K,Suzue J,Nokawa T,Fukuda K,Endo S,Tayama M,Tamura Y,Miyao M

    更新日期:1981-01-01 00:00:00

  • Serotonin transporter gene promoter polymorphism and autism: a family-based genetic association study in Japanese population.

    abstract::Autism is now widely accepted as a biological disorder which, by and large, starts before birth. It has been shown that serotonin (5-HT) is associated with several psychological processes and hyperserotoninemia is observed in some autistic patients. The results of previous reports about family-based association studie...

    journal_title:Brain & development

    pub_type: 杂志文章

    doi:10.1016/j.braindev.2005.09.003

    authors: Koishi S,Yamamoto K,Matsumoto H,Koishi S,Enseki Y,Oya A,Asakura A,Aoki Y,Atsumi M,Iga T,Inomata J,Inoko H,Sasaki T,Nanba E,Kato N,Ishii T,Yamazaki K

    更新日期:2006-05-01 00:00:00

  • Personality and electroencephalography: significance of epileptiform activity on mass screening electroencephalography.

    abstract::From the mass screening EEG, 31 primary school children and 17 junior high school (Jr-HS) students with paroxysmal discharge were chosen. An equal number of children with disorganized patterns, including a few borderline ones, and with normal patterns were selected from the same classes. School performance and behavio...

    journal_title:Brain & development

    pub_type: 杂志文章

    doi:10.1016/s0387-7604(83)80005-9

    authors: Hara H,Tsuchiya S,Maruyama H

    更新日期:1983-01-01 00:00:00

  • The lack of antiepileptic drugs and worsening of seizures among physically handicapped patients with epilepsy during the Great East Japan Earthquake.

    abstract:BACKGROUND:Takuto Rehabilitation Center for Children is located in Sendai, the capital of the Miyagi prefecture, and faces the Pacific Ocean. The tsunami caused by the Great East Japan Earthquake resulted in tremendous damage to this region. Many physically handicapped patients with epilepsy who are treated at our hosp...

    journal_title:Brain & development

    pub_type: 杂志文章

    doi:10.1016/j.braindev.2016.01.005

    authors: Kobayashi S,Endo W,Inui T,Wakusawa K,Tanaka S,Onuma A,Haginoya K

    更新日期:2016-08-01 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

  • Glutamic acid decarboxylase in cerebrospinal fluid in infancy and childhood. Part I. Glutamic acid decarboxylase activity in cerebrospinal fluid of normal infants and children.

    abstract::Glutamic acid decarboxylase (GAD) activity in the cerebrospinal fluid (CSF) of normal infants (n:14) and children (n:28) was determined by measuring the amount of 14CO2 released from L-[1-14C]-glutamic acid. The mean GAD activity in CSF of infants and children was 5.2 +/- 2.5 pmol CO2 formed/hr/ml. Dividing these subj...

    journal_title:Brain & development

    pub_type: 杂志文章

    doi:10.1016/s0387-7604(83)80079-5

    authors: Tada H

    更新日期:1983-01-01 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

  • Outcome of ketogenic diets in GLUT1 deficiency syndrome in Japan: A nationwide survey.

    abstract:OBJECTIVES:To evaluate the outcome of ketogenic diets (KDs) in patients with glucose transport type 1 deficiency syndrome (GLUT1DS) in Japan. METHODS:A nationwide survey for GLUT1DS was conducted by sending questionnaires to board-certified pediatric neurologists nationwide to obtain clinical and laboratory data. RES...

    journal_title:Brain & development

    pub_type: 杂志文章

    doi:10.1016/j.braindev.2016.01.002

    authors: Fujii T,Ito Y,Takahashi S,Shimono K,Natsume J,Yanagihara K,Oguni H

    更新日期:2016-08-01 00:00:00

  • Long-term effectiveness and side effects of acetazolamide as an adjunct to other anticonvulsants in the treatment of refractory epilepsies.

    abstract::The long-term effectiveness of acetazolamide (AZA) and its side effects, especially the formation of renal calculi, were investigated in a prospective study when AZA was used as an adjunct to other antiepileptic drugs in the treatment of refractory epilepsies. The subjects comprised 37 patients aged from 1 to 17 years...

    journal_title:Brain & development

    pub_type: 临床试验,杂志文章

    doi:10.1016/s0387-7604(02)00003-7

    authors: Katayama F,Miura H,Takanashi S

    更新日期:2002-04-01 00:00:00

  • Development of the human abducens nucleus: a morphometric study.

    abstract:BACKGROUND:The abducens nucleus directly innervates the lateral rectus muscle and plays a role in controlling conjugate horizontal eye movements. Although the neuronal cytoarchitecture of the abducens nucleus has been extensively investigated in various species of vertebrates, few studies have been undertaken in humans...

    journal_title:Brain & development

    pub_type: 杂志文章

    doi:10.1016/j.braindev.2011.12.009

    authors: Yamaguchi K,Honma K

    更新日期:2012-10-01 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

  • 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

  • Chromatographic profiles at E-280 nm for urinary precipitates in morbus Rett.

    abstract::Previously we have observed different characteristic chromatographic ultraviolet absorbancy profiles at 280 nm for urinary protein precipitates from patients with behavioral disorders. The purpose with this study was to look for similar changes in urinary protein excretion from the grossly disabled patients with the R...

    journal_title:Brain & development

    pub_type: 杂志文章

    doi:10.1016/s0387-7604(85)80042-5

    authors: Foss I,Hagberg B,Trygstad O

    更新日期:1985-01-01 00:00:00

  • Congenital muscular dystrophy (non-Fukuyama type) in Turkey: a clinical and pathological evaluation.

    abstract::Congenital muscular dystrophy (CMD) is a heterogenous group of disorders. In the majority of cases the intelligence is preserved, which comprises the classic "occidental" (type 1) form. This type appears to be prevalent in the west. We report a five-case series in Turkey, confirming its geographical distribution. ...

    journal_title:Brain & development

    pub_type: 杂志文章

    doi:10.1016/s0387-7604(89)80066-x

    authors: Topaloğlu H,Yalaz K,Renda Y,Kale G,Cağlar M,Göğüş S

    更新日期:1989-01-01 00:00:00

  • Familial pachygyria in both genders related to a DCX mutation.

    abstract::Doublecortin (DCX) and tubulin play critical roles in neuronal migration. DCX mutations usually cause anterior dominant lissencephaly in males and subcortical band heterotopia (SBH) in females. We used whole-exome sequencing to investigate causative gene variants in a large family with late-childhood-onset focal epile...

    journal_title:Brain & development

    pub_type: 杂志文章

    doi:10.1016/j.braindev.2015.12.005

    authors: Kim YO,Nam TS,Park C,Kim SK,Yoon W,Choi SY,Kim MK,Woo YJ

    更新日期:2016-06-01 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

  • Spectrum of MECP2 mutations in Rett syndrome.

    abstract::Mutations in the methyl-CpG-binding protein 2 gene (MECP2) are identified in the majority of females with Rett syndrome (RTT), an X-linked dominant neurodevelopmental disorder. We searched for mutations by sequencing the MECP2 coding region in 45 sporadic cases (35 with classic RTT, eight with variant forms and two ma...

    journal_title:Brain & development

    pub_type: 杂志文章

    doi:10.1016/s0387-7604(01)00339-4

    authors: Lee SS,Wan M,Francke U

    更新日期:2001-12-01 00:00:00

  • Apnea associated with hypoxia in preterm infants: impact on cerebral blood volume.

    abstract::The present study analyzed changes in cerebral blood volume (CBV) during apnea associated with hypoxia compared to apnea without hypoxia. Hypoxia was defined as pulsoxymetric oxygen saturation <80%>10 s. The employed technique was near infrared spectroscopy combined with electrocardiogram, electroocologram, pulsoxymet...

    journal_title:Brain & development

    pub_type: 杂志文章

    doi:10.1016/s0387-7604(02)00121-3

    authors: Payer C,Urlesberger B,Pauger M,Müller W

    更新日期:2003-01-01 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

  • Magnetic resonance studies of brain lesions in patients with Kawasaki disease.

    abstract::We evaluated brain lesions in patients with coronary arterial lesions (CAL) as a complication of Kawasaki disease (KD) by magnetic resonance imaging (MRI) and magnetic resonance angiography (MRA). Among 47 patients who underwent coronary angiography for the evaluation of CAL due to KD at Kyushu University Hospital fro...

    journal_title:Brain & development

    pub_type: 杂志文章

    doi:10.1016/j.braindev.2005.04.003

    authors: Muneuchi J,Kusuhara K,Kanaya Y,Ohno T,Furuno K,Kira R,Mihara F,Hara T

    更新日期:2006-01-01 00:00:00

  • Predictors of unprovoked seizure after febrile seizure: short-term outcomes.

    abstract:INTRODUCTION:We performed this study to confirm the known risk factors and to identify possible new risk factors for subsequent unprovoked seizure after febrile seizure (FS) on Jeju Island, South Korea. METHODS:A population-based retrospective study of 204 children with FS, whose first FS developed between March 2003 ...

    journal_title:Brain & development

    pub_type: 杂志文章

    doi:10.1016/j.braindev.2014.06.003

    authors: Hwang G,Kang HS,Park SY,Han KH,Kim SH

    更新日期:2015-03-01 00:00:00

  • Isolated pyramidal tract impairment in the central nervous system of adult-onset Krabbe disease with novel mutations in the GALC gene.

    abstract::This report describes a 60-year-old female patient with Krabbe disease who presented with slowly progressive gait disturbance due to mild spastic paraplegia. Brain magnetic resonance imaging showed high-intensity lesions along the upper parts of the bilateral pyramidal tracts in fluid-attenuated inversion recovery ima...

    journal_title:Brain & development

    pub_type: 杂志文章

    doi:10.1016/j.braindev.2012.08.004

    authors: Tokushige S,Sonoo T,Maekawa R,Shirota Y,Hanajima R,Terao Y,Matsumoto H,Hossain MA,Sakai N,Shiio Y

    更新日期:2013-06-01 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

  • Retrocerebellar arachnoid cysts in siblings with mental retardation and undescended testis.

    abstract::Arachnoid cysts comprise approximately 1% of all intracranial space-occupying lesions and usually occur sporadically. We report retrocerebellar arachnoid cysts in two male siblings with mental retardation and undescended testis, suggesting the possibility of a genetic basis for at least some cases of retrocerebellar a...

    journal_title:Brain & development

    pub_type: 杂志文章,评审

    doi:10.1016/s0387-7604(02)00061-x

    authors: Suzuki H,Takanashi J,Sugita K,Barkovich AJ,Kohno Y

    更新日期:2002-08-01 00:00:00

  • Abnormalities of joint mobility and gait in children with autism spectrum disorders.

    abstract:AIMS:Abnormalities of gross motor function in children with autism are well known to clinicians but have not received much empirical documentation and, with the exception of stereotypies, are not among its diagnostic criteria. We recorded the characteristics of gait and prevalence of toe walking, the range of passive j...

    journal_title:Brain & development

    pub_type: 杂志文章

    doi:10.1016/j.braindev.2012.02.005

    authors: Shetreat-Klein M,Shinnar S,Rapin I

    更新日期:2014-02-01 00:00:00