Adult fragile X syndrome. Clinico-neuropathologic findings (Q48545759)

From Wikidata

Jump to navigation Jump to search

scientific article

edit

Language	Label	Description	Also known as
English	Adult fragile X syndrome. Clinico-neuropathologic findings	scientific article

Statements

instance of

scholarly article

1 reference

stated in

Europe PubMed Central

PubMed publication ID

4050344

retrieved

12 February 2018

reference URL

http://europepmc.org/abstract/MED/4050344

title

Adult fragile X syndrome. Clinico-neuropathologic findings (English)

1 reference

stated in

Europe PubMed Central

PubMed publication ID

4050344

retrieved

12 February 2018

reference URL

http://europepmc.org/abstract/MED/4050344

main subject

fragile X syndrome

1 reference

based on heuristic

inferred from title

author name string

R D Rudelli

series ordinal

1

1 reference

stated in

Europe PubMed Central

PubMed publication ID

4050344

retrieved

12 February 2018

reference URL

http://europepmc.org/abstract/MED/4050344

W T Brown

series ordinal

2

1 reference

stated in

Europe PubMed Central

PubMed publication ID

4050344

retrieved

12 February 2018

reference URL

http://europepmc.org/abstract/MED/4050344

K Wisniewski

series ordinal

3

1 reference

stated in

Europe PubMed Central

PubMed publication ID

4050344

retrieved

12 February 2018

reference URL

http://europepmc.org/abstract/MED/4050344

E C Jenkins

series ordinal

4

1 reference

stated in

Europe PubMed Central

PubMed publication ID

4050344

retrieved

12 February 2018

reference URL

http://europepmc.org/abstract/MED/4050344

M Laure-Kamionowska

series ordinal

5

1 reference

stated in

Europe PubMed Central

PubMed publication ID

4050344

retrieved

12 February 2018

reference URL

http://europepmc.org/abstract/MED/4050344

F Connell

series ordinal

6

1 reference

stated in

Europe PubMed Central

PubMed publication ID

4050344

retrieved

12 February 2018

reference URL

http://europepmc.org/abstract/MED/4050344

H M Wisniewski

series ordinal

7

1 reference

stated in

Europe PubMed Central

PubMed publication ID

4050344

retrieved

12 February 2018

reference URL

http://europepmc.org/abstract/MED/4050344

publication date

1 January 1985

1 reference

stated in

Europe PubMed Central

PubMed publication ID

4050344

retrieved

12 February 2018

reference URL

http://europepmc.org/abstract/MED/4050344

published in

Acta Neuropathologica

1 reference

stated in

Europe PubMed Central

PubMed publication ID

4050344

retrieved

12 February 2018

reference URL

http://europepmc.org/abstract/MED/4050344

volume

67

1 reference

stated in

Europe PubMed Central

PubMed publication ID

4050344

retrieved

12 February 2018

reference URL

http://europepmc.org/abstract/MED/4050344

issue

3-4

1 reference

stated in

Europe PubMed Central

PubMed publication ID

4050344

retrieved

12 February 2018

reference URL

http://europepmc.org/abstract/MED/4050344

page(s)

289-295

1 reference

stated in

Europe PubMed Central

PubMed publication ID

4050344

retrieved

12 February 2018

reference URL

http://europepmc.org/abstract/MED/4050344

cites work

Testicular biopsy in the study of male infertility.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/4050344

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

X-linked mental retardation and-or hydrocephalus

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/4050344

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

X-linked mental retardation and fragile-X or marker-X syndrome.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/4050344

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A method for the quantitative estimate of Leydig cells in the human testis

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/4050344

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Fragile X syndrome: associated neurological abnormalities and developmental disabilities

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/4050344

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Inherited congenital normofunctional testicular hyperplasia and mental deficiency

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/4050344

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Spine distribution along the apical dendrites of the pyramidal neurons in Down's syndrome. A quantitative Golgi study.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/4050344

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Abnormal neuronal development in the visual cortex of the human fetus and infant with down's syndrome. A quantitative and qualitative Golgi study

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/4050344

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Fragile sites on human chromosomes: demonstration of their dependence on the type of tissue culture medium

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/4050344

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Structural abnormalities of the cerebral cortex in human chromosomal aberrations: a Golgi study

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/4050344

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The aging human Betz cell

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/4050344

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Rapid processing of primary embryonic tissues for chromosome banding pattern analysis.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/4050344

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

X-linked recessively inherited non-specific mental retardation. Report of a large family

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/4050344

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Autism is associated with the fragile-X syndrome

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/4050344

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial sex-linked mental retardation

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/4050344

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The syndrome of sex-linked hydrocephalus

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/4050344

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Screening for fragile X syndrome by testicular size measurement

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/4050344

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Abnormal neuronal differentiation (functional maturation) in mental retardation.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/4050344

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Inherited congenital normofunctional testicular hyperplasia and mental deficiency. A corroborative study

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/4050344

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

X-Linked Mental Deficiency Megalotestes Syndrome

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/4050344

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Neurobiology of Down's syndrome

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/4050344

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Short stature, psychomotor retardation, and unusual facial appearance in two brothers

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/4050344

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

X-linked mental retardation associated with macro-orchidism

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/4050344

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The X-linked syndrome of macroorchidism and mental retardation: Further observations

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/4050344

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Testicular size in fetal fragile X syndrome

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/4050344

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Conference report: International Workshop on the fragile X and X-linked mental retardation.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/4050344

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

X-linked aqueductal stenosis

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/4050344

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Pyramidal cell abnormalities in the motor cortex of a child with Down's syndrome. A Golgi study

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/4050344

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The formation of synaptic junctions in developing rat brain: a quantitative electron microscopic study.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/4050344

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Postnatal development of synaptic contact zones in the visual cortex of rabbits

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/4050344

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Autism and mental retardation: neuropathologic studies performed in four retarded persons with autistic behavior

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/4050344

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Marker (X)-Linked Mental Retardation

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/4050344

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clinical staging of chronic lymphocytic leukemia

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/4050344

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Testicular volume during adolescence. Cross-sectional and longitudinal studies

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/4050344

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The testes in the mentally handicapped.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/4050344

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Testicular changes in association with malformation of the central nervous system and mental retardation

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/4050344

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Diagnosis of the fragile X syndrome (Martin-Bell syndrome). Clinical findings in 27 males with the fragile site at Xq28.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/4050344

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Experience with prenatal fragile X detection

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/4050344

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Dendritic Spine "Dysgenesis" and Mental Retardation

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/4050344

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/4050344

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An X-linked, recessively inherited syndrome characterized by grave mental deficiency, epilepsy, and endocrine disorder

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/4050344

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Effect of prednisolone upon normal and pathologic human spermatogenesis

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/4050344

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Spermiogenesis in elderly men

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/4050344

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

HEREDITARY PARTIAL AGENESIS OF CORPUS CALLOSUM; BIOCHEMICAL AND PATHOLOGICAL STUDIES.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/4050344

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Dendritic development in neocortex of children with mental defect and infantile spasms

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/4050344

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

DOI

10.1007/BF00687814

1 reference

stated in

Europe PubMed Central

PubMed publication ID

4050344

retrieved

12 February 2018

reference URL

http://europepmc.org/abstract/MED/4050344

PubMed publication ID

4050344

1 reference

stated in

Europe PubMed Central

PubMed publication ID

4050344

retrieved

12 February 2018

reference URL

http://europepmc.org/abstract/MED/4050344

 

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

Retrieved from "https://www.wikidata.org/w/index.php?title=Q48545759&oldid=2209575283"