(Q33595575)

English

Childhood onset autosomal dominant polycystic kidney disease in sibs: clinical picture and recurrence risk. German Working Group on Paediatric Nephrology (Arbeitsgemeinschaft für Pädiatrische Nephrologie

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scholarly article

1 reference

Europe PubMed Central

28 July 2017

Childhood onset autosomal dominant polycystic kidney disease in sibs: clinical picture and recurrence risk. German Working Group on Paediatric Nephrology (Arbeitsgemeinschaft für Pädiatrische Nephrologie (English)

1 reference

Europe PubMed Central

28 July 2017

autosomal dominant polycystic kidney disease

0 references

autosomal dominant polycystic kidney

1 reference

based on heuristic

inferred from title

author name string

Zerres K

1

1 reference

Europe PubMed Central

28 July 2017

Rudnik-Schöneborn S

2

1 reference

Europe PubMed Central

28 July 2017

Deget F

3

1 reference

Europe PubMed Central

28 July 2017

language of work or name

0 references

publication date

1 July 1993

1 reference

Europe PubMed Central

28 July 2017

Journal of Medical Genetics

1 reference

Europe PubMed Central

28 July 2017

30

1 reference

Europe PubMed Central

28 July 2017

583-588

1 reference

Europe PubMed Central

28 July 2017

7

1 reference

Europe PubMed Central

28 July 2017

Sotos syndrome with intestinal polyposis and pigmentary changes of the genitalia.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016459

21 June 2018

The syndromes of Marshall and Weaver.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016459

21 June 2018

A Weaver-like syndrome in a Japanese boy.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016459

21 June 2018

Weaver-Smith syndrome. A case study with long-term follow-up

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016459

21 June 2018

Letter: Optimal antibiotic and antitoxin treatment of tetanus?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016459

21 June 2018

A new overgrowth syndrome with accelerated skeletal maturation, unusual facies, and camptodactyly

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016459

21 June 2018

Weaver syndrome with pes cavus.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016459

21 June 2018

Update on the Marshall-Smith-Weaver controversy.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016459

21 June 2018

A girl with the Weaver syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016459

21 June 2018

Weaver syndrome: the changing phenotype in an adult.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016459

21 June 2018

A comprehensive and critical assessment of overgrowth and overgrowth syndromes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016459

21 June 2018

Further delineation of Weaver syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016459

21 June 2018

Weaver syndrome and instability of the upper cervical spine.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016459

21 June 2018

Psychological characteristics of Sotos syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016459

21 June 2018

Acceleration of postnatal development, hypertony, enlargement of the middle phalanges and of the distal metaphyses of the femur, peculiar facies: a case of Weaver's syndrome?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016459

21 June 2018

Accelerated bone maturation syndrome of the Weaver type.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016459

30 October 2018

The Weaver syndrome: a rare type of primordial overgrowth.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016459

30 October 2018

Siblings with Weaver syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016459

30 October 2018

The Weaver-Smith syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/8411032

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Two children with cerebral gigantism and congenital primary hypothyroidism

1 reference

https://pubmed.ncbi.nlm.nih.gov/8411032

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The Weaver syndrome in a girl

1 reference

https://pubmed.ncbi.nlm.nih.gov/8411032

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[Acceleration of bone maturation and dysmorphic syndrome in 2 siblings (Marshall-Weaver syndrome)]

1 reference

https://pubmed.ncbi.nlm.nih.gov/8411032

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A new autosomal recessive disorder resembling Weaver syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/8411032

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A Weaver-like syndrome with endocrinological abnormalities in a boy and his mother

1 reference

https://pubmed.ncbi.nlm.nih.gov/8411032

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1136/JMG.30.7.583

1 reference

Europe PubMed Central

28 July 2017

1 reference

Europe PubMed Central

28 July 2017

1 reference

Europe PubMed Central

28 July 2017

ResearchGate publication ID

0 references

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