(Q28273623)

https://api.crossref.org/works/10.1007%2FS004310050830

The MASA syndrome: A new heritable mental retardation syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS004310050830

Mild fetal lateral cerebral ventriculomegaly: clinical course and outcome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS004310050830

Outcome of fetal ventriculomegaly

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS004310050830

Congenital absence of pyramids and its significance in genetic diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS004310050830

Autosomal recessive hydrocephalus with third ventricle obstruction

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS004310050830

Management of Pregnant Women with Cerebrospinal Fluid Shunts

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS004310050830

The syndrome of sex-linked hydrocephalus

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS004310050830

Epidemiology of infantile hydrocephalus in Sweden. I. Birth prevalence and general data

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS004310050830

Epidemiology of infantile hydrocephalus in Sweden. II. Origin in infants born at term.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS004310050830

Natural history of X-linked aqueductal stenosis in the second and third trimesters of pregnancy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS004310050830

X linked complicated spastic paraplegia, MASA syndrome, and X linked hydrocephalus owing to congenital stenosis of the aqueduct of Sylvius: variable expression of the same mutation at Xq28

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS004310050830

A new view on the CSF-circulation with the potential for pharmacological treatment of childhood hydrocephalus

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS004310050830

Etiologic heterogeneity of fetal hydrocephalus diagnosed by ultrasound.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS004310050830

Molecular structure and functional testing of human L1CAM: an interspecies comparison

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS004310050830

Prenatal diagnosis and management of fetal hydrocephaly and lissencephaly

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS004310050830

Refining the genetic location of the gene for X linked hydrocephalus within Xq28.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS004310050830

New domains of neural cell-adhesion molecule L1 implicated in X-linked hydrocephalus and MASA syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS004310050830

Linkage studies of X-linked recessive spastic paraplegia using DNA probes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS004310050830

X linked hydrocephalus and MASA syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS004310050830

Long-term outcome of fetal hydrocephaly.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS004310050830

Clasped-thumb mental retardation (MASA) syndrome: confirmation of linkage to Xq28.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS004310050830

Prenatal hydrocephalus: outcome and prognosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS004310050830

Aberrant splicing of neural cell adhesion molecule L1 mRNA in a family with X-linked hydrocephalus

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS004310050830

21 January 2018

Hydrolethalus syndrome

1 reference

https://api.crossref.org/works/10.1007%2FS004310050830

MASA syndrome: new clinical features and linkage analysis using DNA probes

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS004310050830

Fetal biometry at 14-40 weeks' gestation

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS004310050830

Regulation of axonal growth in the vertebrate nervous system by interactions between glycoproteins belonging to two subgroups of the immunoglobulin superfamily

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS004310050830

An epidemiologic study of environmental and genetic factors in congenital hydrocephalus

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS004310050830

Transvaginal sonographic detection of adducted thumbs, hydrocephalus, and agenesis of the corpus callosum at 22 postmenstrual weeks: the masa spectrum or L1 spectrum. A case report and review of the literature

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS004310050830

Calcium influx into neurons can solely account for cell contact-dependent neurite outgrowth stimulated by transfected L1

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS004310050830

Activation of the FGF receptor underlies neurite outgrowth stimulated by L1, N-CAM, and N-cadherin

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS004310050830

MASA syndrome: further clinical delineation and chromosomal localisation

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS004310050830

Mutations in the cell adhesion molecule L1 cause mental retardation

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS004310050830

Functional expression of a full-length cDNA coding for rat neural cell adhesion molecule L1 mediates homophilic intercellular adhesion and migration of cerebellar neurons

21 January 2018

1 reference

12 December 2020

VACTERL with hydrocephalus in twins due to Fanconi anemia (FA): mutation in the FAC gene

1 reference

12 December 2020

Understanding the molecules of neural cell contacts: emerging patterns of structure and function

1 reference

12 December 2020

Agenesis of the corpus callosum associated with MASA syndrome.

1 reference

12 December 2020

CONSECUTIVE HYDROCEPHALUS: REPORT OF 2 CASES

1 reference

12 December 2020

Autosomal recessive nonsyndromal hydrocephalus

1 reference

12 December 2020

L1-mediated axon outgrowth occurs via a homophilic binding mechanism

1 reference

12 December 2020

Congenital hydrocephalus: a review and protocol for perinatal management

1 reference

12 December 2020

Gene analysis of L1 neural cell adhesion molecule in prenatal diagnosis of hydrocephalus

1 reference

12 December 2020

Fetal hydrocephalus: diagnosis and management

1 reference

12 December 2020

Aqueductal Stenosis in X-Linked Hydrocephalus: a Secondary Phenomenon?

1 reference

12 December 2020

The epidemiology of congenital hydrocephalus. A study in Brooklyn, N.Y. 1968--1976

1 reference

12 December 2020

Autosomal recessive congenital stenosis of aqueduct of Sylvius.

1 reference

12 December 2020

[Congenital stenosis of the aqueduct of Sylvius transmitted in an autosomal recessive mode (5 cases in 2 families)]

1 reference

12 December 2020

Prenatal diagnosis of X linked hydrocephalus without aqueductal stenosis

1 reference

12 December 2020

Maternal neurosurgical shunts and pregnancy outcome.

1 reference

12 December 2020

A family study of hydrocephalus resulting from aqueduct stenosis

1 reference

12 December 2020

Recurrence risks for congenital hydrocephalus

1 reference

12 December 2020

Family study of congenital hydrocephalus

1 reference

12 December 2020

Walker-Warburg syndrome (Warburg syndrome, HARD +/- E syndrome)

1 reference

12 December 2020

Clinical aspects of the MASA syndrome in a large family, including expressing females.

1 reference

12 December 2020

X linked hydrocephalus: a survey of a 20 year period in Victoria, Australia

1 reference

12 December 2020

Familial hydrocephalus of prenatal onset

1 reference

12 December 2020

The MASA syndrome: a new heritable mental retardation syndrome

1 reference

12 December 2020

Heterogeneity and recurrence risk for congenital hydrocephalus (Ventriculomegaly): A prospective study

1 reference

12 December 2020

A proposed model of cerebrospinal fluid circulation: observations with radionuclide cisternography.

1 reference

12 December 2020

Intrauterine hydrocephalus and ventriculomegaly: associated anomalies and fetal outcome

1 reference

12 December 2020

[Poor prognosis in children with ultrasonographically diagnosed abnormalities of the central nervous system]

1 reference

12 December 2020

[Repeated congenital hydrocephalus]

1 reference

12 December 2020

A clinical and neuroradiological study of X-linked hydrocephalus in Japan

1 reference

12 December 2020

X-linked hydrocephalus

1 reference

12 December 2020

Three hydrocephalic newborns-each of a successive pregnancy of a white female

1 reference

12 December 2020

[Multidisciplinary assessment of the fetus with hydrocephalus: study protocol and results]

1 reference

12 December 2020

Hereditary stenosis of the aqueduct of Sylvius as a cause of congenital hydrocephalus.

1 reference

12 December 2020

1 reference

12 December 2020