(Q45159053)

10 December 2017

title

Studies of malformation syndromes of man XXIX: the Wiedemann-Beckwith syndrome. Clinical, genetic and pathogenetic studies of 12 cases (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A976281

11 August 2022

6

J M Opitz

1 reference

10 December 2017

A. L. Kosseff

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A976281

11 August 2022

J. Herrmann

2

1 reference

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11 August 2022

E. F. Gilbert

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A976281

11 August 2022

C. Viseskul

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A976281

11 August 2022

M. Lubinsky

5

1 reference

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11 August 2022

language of work or name

English

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=976281

11 August 2022

publication date

1 October 1976

1 reference

European Journal of Pediatrics

10 December 2017

published in

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10 December 2017

volume

123

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10 December 2017

issue

3

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10 December 2017

page(s)

139-166

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Macroglossia, abnormal umbilicus and hypoglycaemia (Beckwith’s syndrome)

10 December 2017

cites work

1 reference

12 December 2020

[A case of exomphalos-macroglossia-gigantism]

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12 December 2020

1 reference

12 December 2020

Familial occurrence of omphalocele

1 reference

12 December 2020

Metabolic aspects of the Beckwith-Wiedemann syndrome

1 reference

12 December 2020

[Exomphalos-macroglossia-gigantism syndrome (Wiedemann-Beckwith syndrome) in three siblings]

1 reference

12 December 2020

An (X;1) translocation, balanced, 46 chromosomes. Repository identification no. GM-97.

1 reference

12 December 2020

Syndrome of fetal gigantism, renal hamartomas, and nephroblastomatosis with Wilms' tumor

1 reference

12 December 2020

The Beckwith-Wiedmann syndrome

1 reference

12 December 2020

Adrenogenital syndrome in a male child due to adrenocortical tumor; report of case with hemihypertrophy and subsequent development of embryoma (Wilms' tumor)

1 reference

12 December 2020

Wilms' tumor and congenital hemihypertrophy: report of five new cases and review of literature.

1 reference

12 December 2020

On the "Kerben-Ohr" (inherited slit-like indentations of ear-lobes) in the Exomphalos-Macroglossia-Gigantism Syndrome, on auricular fistulae and on the presence of analogous findings in other syndromes and in normal individuals (author's transl)

1 reference

12 December 2020

Pseudohermaphroditism, nephron disorder and wilms' tumor: a unifying concept

1 reference

12 December 2020

Letter: Autosomal-dominant sex-dependent transmission of the Wiedemann-Beckwith syndrome

1 reference

12 December 2020

New syndrome of neonatal hypoglycemia. Association with visceromegaly, macroglossia, microcephaly and abnormal umbilicus

1 reference

12 December 2020

Immunodeficiency associated with exomphalos-macroglossia-gigantism syndrome

1 reference

12 December 2020

Syndrome of hyperplastic fetal visceromegaly and neonatal hypoglycemia (Beckwith's syndrome). A report of seven cases

1 reference

12 December 2020

Exomphalos-Macroglossia-Gigantism Syndrome in Jamaican Infants

1 reference

12 December 2020

Macroglossia, omphalocele, visceromegaly, cytomegaly of the adrenal cortex and neonatal hypoglycemia.

1 reference

12 December 2020

Further studies of the hypoglycemia in children with the exomphalos--macroglossia--gigantism syndrome

1 reference

12 December 2020

Syndrome of excessive growth with macroglossia and omphalocele (Widedeman-Beckwith)

1 reference

12 December 2020

Nesidioblastosis in Beckwith syndrome

1 reference

12 December 2020

Congenital anomalies in children with Wilms' Tumor. A new survey

1 reference

12 December 2020

Deficient 17-Hydroxylation in a Corticosterone Producing Adrenal Tumor from an Infant with Hemihypertrophy and Visceromegaly1

1 reference

12 December 2020

Chromosomal abnormality associated with congenital macroglossia and other abnormalities

1 reference

12 December 2020

Radiology of the Beckwith-Wiedemann syndrome

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12 December 2020

Adrenocortical neoplasms with hemihypertrophy, brain tumors, and other disorders.

1 reference

12 December 2020

Neoplasms associated with the Beckwith-Wiedemann syndrome

1 reference

12 December 2020

Omphalocele in siblings; report of two cases with surgical recovery

1 reference

12 December 2020

Exomphalos with macroglossia: a study of eleven cases.

1 reference

12 December 2020

Primary carcinoma of the liver in childhood: an epidemiologic study

1 reference

12 December 2020

Congenital hemihypertrophy and malignancy

1 reference

12 December 2020

Epithelial hepatoblastoma associated with congenital hemihypertrophy and cystathioninuria: presentation of a case.

1 reference

12 December 2020

Beckwith-Wiedemann syndrome. Wilms' tumor, cardiac hamartoma, persistent visceromegaly, and glomeruloneogenesis in a 2-year-old boy.

1 reference

12 December 2020

Wiedemann-Beckwith syndrome

1 reference

12 December 2020

1 reference

12 December 2020

Letter: Pseudo-Beckwith-Wiedemann syndrome: interaction with maternal diabetes

1 reference

12 December 2020

Nuclei from rat liver: isolation method that combines purity with high yield

1 reference

12 December 2020

The Wiedemann-Beckwith syndrome: genetic considerations and a diagnostic sign.

1 reference

12 December 2020

Renal hamartomas and nephroblastomatosis with fetal gigantism: a familial syndrome

1 reference

12 December 2020

FAMILIAL MALFORMATION COMPLEX WITH UMBILICAL HERNIA AND MACROGLOSSIA--A "NEW SYNDROME"?

1 reference

12 December 2020

ASSOCIATION OF WILMS'S TUMOR WITH ANIRIDIA, HEMIHYPERTROPHY AND OTHER CONGENITAL MALFORMATIONS

1 reference

12 December 2020

Wiedemann-Beckwith syndrome (omphalocele-macroglossia-gigantism)

1 reference

12 December 2020

A microchemical determination of desoxyribonucleic acid

1 reference

12 December 2020

EMG syndrome, Berardinelli-Seip syndrome, and Sotos' syndrome--comparison of special aspects (author's transl)

1 reference

12 December 2020

Congenital metastasizing adrenal cortical carcinoma associated with cytomegaly of the fetal adrenal cortex

1 reference

12 December 2020

Hepatoblastoma and hepatocarcinoma in infancy and childhood. Report of 47 cases

1 reference

12 December 2020

[Wilms' tumor and aniridia--a genetically determined syndrome?]

1 reference

12 December 2020

The EMG-syndrome: Exomphalos, macroglossia, gigantism and disturbed carbohydrate metabolism

1 reference

12 December 2020

Macroglossia, transient neonatal diabetes mellitus and intrauterine growth failure: a new distinct entity?

1 reference

12 December 2020

Adrenocortical carcinoma and congenital hemihypertrophy

1 reference

12 December 2020

Wilms's tumor in three children of a woman with congenital hemihypertrophy.

1 reference

12 December 2020

The "E.M.G." syndrome (Exomphalos, Macroglossia, Gigantism).

1 reference

12 December 2020

Beckwith's syndrome with extreme organ hyperplasia

1 reference

12 December 2020

Dermatoglyphics in children with embryonic tumors (author's transl)

1 reference

12 December 2020

Cytomegaly of the adrenal cortex. Electron microscopy in Beckwith's syndrome

1 reference

12 December 2020

Letter: Wiedemann-Beckwith syndrome

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF00452093

1 reference

Dimensions Publication ID

10 December 2017

1052617878

0 references

1 reference