(Q39518276)

12 September 2017

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title

Wiedemann-Beckwith syndrome. (English)

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12 September 2017

W Engström

1

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PubMed ID

3044795

12 September 2017

S Lindham

series ordinal

2

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PubMed ID

3044795

12 September 2017

P Schofield

series ordinal

3

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12 September 2017

1 June 1988

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European Journal of Pediatrics

12 September 2017

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12 September 2017

147

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12 September 2017

450-457

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12 September 2017

5

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https://scigraph.springernature.com/pub.10.1007/bf00441965

12 September 2017

0 references

cites work

Nesidioblastosis in Beckwith syndrome

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FBF00441965

Pancreoblastoma in a neonate associated with Beckwith-Wiedemann syndrome

21 January 2018

1 reference

12 December 2020

Monozygotic twins discordant for Wiedemann-Beckwith syndrome and the implications for genetic counselling.

1 reference

12 December 2020

Beckwith-Wiedemann syndrome. Clinical comparison between patients with and without 11p15 trisomy

1 reference

12 December 2020

[Somatomedin activity in Wiedemann-Beckwith syndrome]

1 reference

12 December 2020

The birth prevalence of malformation syndromes in Tokyo infants: a survey of 14,430 newborn infants

1 reference

12 December 2020

Insulin-like growth factors (IGF) 1 and 2 in human foetal plasma and relationship to gestational age and foetal size during midpregnancy

1 reference

12 December 2020

The Beckwith-Wiedemann syndrome. The exomphalos-macroglossia-gigantism syndrome.

1 reference

12 December 2020

Insulin-like growth factor (IGF)/somatomedin receptor subtypes: structure, function, and relationships to insulin receptors and IGF carrier proteins

1 reference

12 December 2020

Metabolic aspects of the Beckwith-Wiedemann syndrome

1 reference

12 December 2020

Normal dosage of the insulin and insulin-like growth factor II genes in patients with the Beckwith-Wiedemann syndrome.

1 reference

12 December 2020

Plasma somatomedin activity in an infant with Beckwith Wiedemann syndrome

1 reference

12 December 2020

Massive infantile nephroblastomatosis.A clinical, radiological, and pathological analysis of four cases

1 reference

12 December 2020

Nephroblastoma and Beckwith-Wiedemann syndrome

1 reference

12 December 2020

Introduction of a normal human chromosome 11 into a Wilms' tumor cell line controls its tumorigenic expression

1 reference

12 December 2020

The Beckwith-Wiedmann syndrome

1 reference

12 December 2020

Insulin-like growth factors/somatomedins: structure, secretion, biological actions and physiological role

1 reference

12 December 2020

E.M.G. syndrome and carbohydrate metabolism

1 reference

12 December 2020

The Beckwith-Wiedemann syndrome: a longitudinal study of the macroglossia and dentofacial complex

1 reference

12 December 2020

Growth and Somatomedins

1 reference

12 December 2020

Immunodeficiency associated with exomphalos-macroglossia-gigantism syndrome

1 reference

12 December 2020

The basic structural lesion of persistent neonatal hypoglycaemia with hyperinsulinism: deficiency of pancreatic D cells or hyperactivity of B cells?

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

ACTH in normal children and children with pituitary and adrenal diseases. I. Measurement in plasma by radioimmunoassay--basal values

1 reference

12 December 2020

Regulation by growth hormone of number of chondrocytes containing IGF-I in rat growth plate

1 reference

12 December 2020

Molecular analysis of chromosome 11 deletions in aniridia-Wilms tumor syndrome

1 reference

12 December 2020

Somatomedin-c in the Beckwith-Wiedemann syndrome

1 reference

12 December 2020

Macroglossia as a presentation of the Beckwith-Wiedemann syndrome

1 reference

12 December 2020

Breast fibroadenoma and cardiac anomaly associated with EMG (Beckwith-Wiedemann) syndrome

1 reference

12 December 2020

Regulation of human IGF-II transcription in fetal and adult tissues

1 reference

12 December 2020

Chronic alveolar hypoventilation secondary to macroglossia in the Beckwith-Wiedemann syndrome

1 reference

12 December 2020

The Wiedemann-Beckwith syndrome: pedigree studies on five families with evidence for autosomal dominant inheritance with variable expressivity

1 reference

12 December 2020

Beckwith-Wiedemann syndrome: role of ultrasound in its management

1 reference

12 December 2020

Neoplasms associated with the Beckwith-Wiedemann syndrome

1 reference

12 December 2020

A human DNA segment with properties of the gene that predisposes to retinoblastoma and osteosarcoma

1 reference

12 December 2020

Beckwith-Wiedemann syndrome: prenatal ultrasound diagnosis using standard kidney to abdominal circumference ratio

1 reference

12 December 2020

Regulation of somatomedin-C/insulin-like growth factor I by nutrients.

1 reference

12 December 2020

Exomphalos with macroglossia: a study of eleven cases.

1 reference

12 December 2020

The Wiedemann-Beckwith syndrome in four sibs including one with associated congenital hypothyroidism

1 reference

12 December 2020

Somatomedin (insulin-like growth factors)-binding proteins. Molecular forms and regulation

1 reference

12 December 2020

Analysis of gene dosage on chromosome 11 in children suffering from Beckwith-Wiedemann syndrome.

1 reference

12 December 2020

Association of the Beckwith — Wiedemann and Prune Belly Syndromes

1 reference

12 December 2020

Trisomy 11p15 and Beckwith-Wiedemann syndrome. A report of two cases.

1 reference

12 December 2020

Medullary sponge kidney and partial Beckwith-Wiedemann Syndrome associated with congenital asymmetry

1 reference

12 December 2020

Effect of insulin-like growth factor on collagen and glycosaminoglycan synthesis by rabbit articular chondrocytes in culture

1 reference

12 December 2020

Trisomy 11p15 and Beckwith-Wiedemann syndrome. Report of two new cases

1 reference

12 December 2020

The pre and postnatal appearance of the kidneys in Beckwith-Wiedemann Syndrome

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

Abnormality of chromosome 11 in patients with features of Beckwith-Wiedemann syndrome

1 reference

12 December 2020

Beckwith-Wiedemann syndrome: a quantitative, immunohistochemical study of pancreatic islet cell populations

1 reference

12 December 2020

Loss of alleles at loci on human chromosome 11 during genesis of Wilms' tumour

1 reference

12 December 2020

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

1 reference

12 December 2020

Regulation of amino acid uptake and deoxyribonucleic acid synthesis in isolated human fetal fibroblasts and myoblasts: effect of human placental lactogen, somatomedin-C, multiplication-stimulating activity, and insulin

1 reference

12 December 2020

Growth factors in embryogenesis

1 reference

12 December 2020

Focal giant cell cardiomyopathy with Beckwith-Wiedemann syndrome

1 reference

12 December 2020

Insulin-like growth factor-II gene expression in Wilms' tumour and embryonic tissues.

1 reference

12 December 2020

Complete and incomplete forms of Beckwith-Wiedemann syndrome: their oncogenic potential

1 reference

12 December 2020

Cardiovascular abnormalities in the Beckwith-Wiedemann syndrome

1 reference

12 December 2020

Excretion of polyamines by children with Beckwith's syndrome

1 reference

12 December 2020

Neuroblastoma associated with Beckwith-Wiedemann syndrome

1 reference

12 December 2020

1 reference

12 December 2020

Thyroxine-binding globulin deficiency in Beckwith syndrome

1 reference

12 December 2020

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

1 reference

12 December 2020

Developmental patterns of insulin-like growth factor-I and -II synthesis and regulation in rat fibroblasts

1 reference

12 December 2020

Racial variation in incidence of Wilms' tumor: Relationship to congenital anomalies

1 reference

12 December 2020

Early tongue resection for Beckwith-Wiedemann macroglossia

1 reference

12 December 2020

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

1 reference

12 December 2020

Wiedemann-Beckwith syndrome in one of monozygotic twins

1 reference

12 December 2020

Loss of heterozygosity in three embryonal tumours suggests a common pathogenetic mechanism

1 reference

12 December 2020

Raised somatomedin associated with normal growth hormone. A cause of Beckwith-Wiedemann syndrome?

1 reference

12 December 2020

Wilms' tumor and adrenocortical carcinoma with hemihypertrophy and hamartomas

1 reference

12 December 2020

Adrenal calcification in Beckwith-Wiedemann syndrome

1 reference

12 December 2020

In utero diagnosis of Beckwith--Wiedemann syndrome by ultrasound

1 reference

12 December 2020

Massive thymic hyperplasia in an infant with Beckwith-Wiedemann syndrome

1 reference

12 December 2020

The macroglossia of Beckwith's syndrome

1 reference

12 December 2020

Prenatal diagnosis of the Beckwith-Wiedemann syndrome

1 reference

12 December 2020

Preferential enhancement of myoblast differentiation by insulin-like growth factors (IGF I and IGF II) in primary cultures of chicken embryonic cells

1 reference

12 December 2020

Renal ultrasonography in Beckwith-Wiedemann syndrome

1 reference

12 December 2020

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

1 reference

12 December 2020

Wilms' tumor in a patient with an incomplete form of Beckwith-Wiedemann syndrome

1 reference

12 December 2020

Somatomedin activity in human cord plasma and relationship to birth size, insulin, growth hormone, and prolactin

1 reference

12 December 2020

A variant of the Wiedemann-Beckwith syndrome

1 reference

12 December 2020

The placenta in familial beckwith-wiedemann syndrome

1 reference

12 December 2020

Beckwith's syndrome with extreme organ hyperplasia

1 reference

12 December 2020

Linkage map of the short arm of human chromosome 11: location of the genes for catalase, calcitonin, and insulin-like growth factor II.

1 reference

12 December 2020

Letter: Wiedemann-Beckwith syndrome

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF00441965

1 reference

12 September 2017

1 reference

PubMed ID

3044795