Home
Random
Nearby
Log in
Settings
Donate
About Wikidata
Disclaimers
Search
(Q48432385)
Watch
English
Non-progressive congenital ataxias
scientific article published in June 1998
In more languages
edit
Statements
instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9661964
retrieved
11 February 2018
reference URL
http://europepmc.org/abstract/MED/9661964
review article
1 reference
stated in
Europe PubMed Central
title
Non-progressive congenital ataxias
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9661964
retrieved
11 February 2018
reference URL
http://europepmc.org/abstract/MED/9661964
author name string
Steinlin M
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9661964
retrieved
11 February 2018
reference URL
http://europepmc.org/abstract/MED/9661964
publication date
1 June 1998
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9661964
retrieved
11 February 2018
reference URL
http://europepmc.org/abstract/MED/9661964
published in
Brain and Development
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9661964
retrieved
11 February 2018
reference URL
http://europepmc.org/abstract/MED/9661964
volume
20
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9661964
retrieved
11 February 2018
reference URL
http://europepmc.org/abstract/MED/9661964
issue
4
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9661964
retrieved
11 February 2018
reference URL
http://europepmc.org/abstract/MED/9661964
page(s)
199-208
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9661964
retrieved
11 February 2018
reference URL
http://europepmc.org/abstract/MED/9661964
cites work
Non-progressive ataxia: origins, brain pathology and impairments in 78 swedish children.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0387-7604%2898%2900019-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Cognitive and language functions of the human cerebellum
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0387-7604%2898%2900019-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A clinical classification of hereditary ataxias
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0387-7604%2898%2900019-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Subtotal agenesis of the cerebellum in an adult. MRI demonstration
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0387-7604%2898%2900019-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Human cerebellar hypoplasia: a syndrome of diverse causes
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0387-7604%2898%2900019-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Congenital granuloprival hypoplasia of cerebellar and hippocampal cortex
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0387-7604%2898%2900019-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Primary degeneration of the granular layer of the cerebellum. A study of 14 patients and review of the literature
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0387-7604%2898%2900019-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Autosomal recessive cerebellar hypoplasia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0387-7604%2898%2900019-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Nosology of congenital non-progressive cerebellar ataxia. Report on six cases in three families
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0387-7604%2898%2900019-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Autosomal recessive congenital cerebellar hypoplasia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0387-7604%2898%2900019-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Symmetrical hypogenesis of the cerebellum
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0387-7604%2898%2900019-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Congenital Ataxic Syndromes in Cerebral Pals
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0387-7604%2898%2900019-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Nonprogressive cerebellar disorder with mental retardation and autosomal recessive inheritance in Hutterites
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0387-7604%2898%2900019-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Infantile cerebellar atrophy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0387-7604%2898%2900019-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Dominantly inherited early-onset non-progressive cerebellar ataxia syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0387-7604%2898%2900019-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
An extended phenotype of an early-onset inherited nonprogressive cerebellar ataxia syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0387-7604%2898%2900019-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Dominantly inherited hypoplasia of the vermis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0387-7604%2898%2900019-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Dominantly inherited congenital cerebellar ataxia with atrophy of the vermis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0387-7604%2898%2900019-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Familial cerebral palsy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0387-7604%2898%2900019-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Sex-linked recessive congenital ataxia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0387-7604%2898%2900019-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Autosomal recessive non-progressive ataxia with an early childhood debut
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0387-7604%2898%2900019-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Pontocerebellar hypoplasias. An overview of a group of inherited neurodegenerative disorders with fetal onset
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0387-7604%2898%2900019-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Dandy-Walker syndrome and agenesis of the cerebellar vermis: diagnostic problems and genetic counselling
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0387-7604%2898%2900019-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The Dandy-Walker malformation. A review of 40 cases
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0387-7604%2898%2900019-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Vascular and nonvascular intracranial malformation associated with external capillary hemangiomas
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0387-7604%2898%2900019-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Ataxia, developmental delay and an extensive neuronal migration abnormality in 2 siblings.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0387-7604%2898%2900019-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Familial agenesis of the cerebellar vermis. A syndrome of episodic hyperpnea, abnormal eye movements, ataxia, and retardation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0387-7604%2898%2900019-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Joubert Syndrome: Episodic Hyperpnea, Abnormal Eye Movements, Retardation and Ataxia, Associated with Dysplasia of the Cerebellar Vermis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0387-7604%2898%2900019-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Joubert syndrome: a review
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0387-7604%2898%2900019-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Follow-up in children with Joubert syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0387-7604%2898%2900019-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The Joubert syndrome associated with bilateral chorioretinal coloboma.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0387-7604%2898%2900019-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Hereditary syndrome of congenital retinal blindness (Leber), polycystic kidneys and maldevelopment of the brain
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0387-7604%2898%2900019-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Further delineation of a syndrome of cerebellar vermis hypo/aplasia, oligophrenia, congenital ataxia, coloboma, and hepatic fibrosis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0387-7604%2898%2900019-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Oral-facial-digital syndrome type VI (Váradi syndrome): further clinical delineation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0387-7604%2898%2900019-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Syndrome of polydactyly, cleft lip/palate or lingual lump, and psychomotor retardation in endogamic gypsies.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0387-7604%2898%2900019-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
ANIRIDIA, CEREBELLAR ATAXIA, AND OLIGOPHRENIA IN SIBLINGS.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0387-7604%2898%2900019-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Genomic structure, evolutionary conservation and aniridia mutations in the human PAX6 gene
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0387-7604%2898%2900019-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
X-linked nonprogressive congenital cerebellar hypoplasia: clinical description and mapping to chromosome Xq.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0387-7604%2898%2900019-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Congenital cerebellar hypoplasia and hypogonadotropic hypogonadism.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0387-7604%2898%2900019-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Autosomal recessive cerebellar hypoplasia and endosteal sclerosis: A newly recognized syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0387-7604%2898%2900019-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Cerebellar hypoplasia, communicating hydrocephalus and mental retardation in two brothers and a maternal uncle.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0387-7604%2898%2900019-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Congenital hypoplastic thrombocytopenia and cerebral malformations in two brothers
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0387-7604%2898%2900019-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A syndrome of progressive pancytopenia with microcephaly, cerebellar hypoplasia and growth failure
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0387-7604%2898%2900019-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Congenital X-linked ataxia, progressive myoclonic encephalopathy, macular degeneration and recurrent infections
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0387-7604%2898%2900019-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Evaluation of familial biochemically determined mental retardation in children, with special reference to aminoaciduria.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0387-7604%2898%2900019-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A sibship with a neuronal migration defect, cerebellar hypoplasia and congenital lymphedema
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0387-7604%2898%2900019-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Dandy-Walker(like) malformation, atrio-ventricular septal defect and a similar pattern of minor anomalies in 2 sisters: a new syndrome?
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0387-7604%2898%2900019-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Another case of Ritscher-Schinzel-syndrome: craniocerebello-cardiac dysplasia (3C-syndrome) with associated bilateral colobomata
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0387-7604%2898%2900019-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Evidence for Ritscher‐Schinzel syndrome in Canadian native Indians
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0387-7604%2898%2900019-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
‘Puppet’ Children A Report on Three Cases
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0387-7604%2898%2900019-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Angelman's syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0387-7604%2898%2900019-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Compensatory head tilt in upbeating nystagmus
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0387-7604%2898%2900019-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Leber's congenital amaurosis. A retrospective study of 33 cases and a histopathological study of one case
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0387-7604%2898%2900019-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Congenital cytomegalovirus infection
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0387-7604%2898%2900019-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Late intrauterine Cytomegalovirus infection: clinical and neuroimaging findings
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0387-7604%2898%2900019-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Dandy-Walker malformation: etiologic heterogeneity and empiric recurrence risks
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0387-7604%2898%2900019-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The vestibulo-ocular reflex in pupils at a Dutch school for the hearing impaired; findings relating to acquired causes.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0387-7604%2898%2900019-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Vestibular deficits in deaf children
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0387-7604%2898%2900019-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Cerebellar involvement in metabolic disorders: a pattern-recognition approach
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0387-7604%2898%2900019-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The Mohr syndrome: are there two variants?
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0387-7604%2898%2900019-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Oto-palatal-digital syndrome type II with X-linked cerebellar hypoplasia/hydrocephalus
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0387-7604%2898%2900019-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Early neurological manifestations and brain anomalies in Marden-Walker syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0387-7604%2898%2900019-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The Klippel-Feil syndrome: genetic and clinical reevaluation of cervical fusion
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0387-7604%2898%2900019-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Cerebellar hypoplasia in a patient with velo-cardio-facial syndrome.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0387-7604%2898%2900019-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The Dandy-Walker syndrome. A clinicopathological study based on 28 cases
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0387-7604%2898%2900019-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1016/S0387-7604(98)00019-9
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9661964
retrieved
11 February 2018
reference URL
http://europepmc.org/abstract/MED/9661964
PubMed publication ID
9661964
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9661964
retrieved
11 February 2018
reference URL
http://europepmc.org/abstract/MED/9661964
Sitelinks
Wikipedia
(0 entries)
edit
Wikibooks
(0 entries)
edit
Wikinews
(0 entries)
edit
Wikiquote
(0 entries)
edit
Wikisource
(0 entries)
edit
Wikiversity
(0 entries)
edit
Wikivoyage
(0 entries)
edit
Wiktionary
(0 entries)
edit
Multilingual sites
(0 entries)
edit