(Q41928134)

English

Microcephaly and early-onset nephrotic syndrome--confusion in Galloway-Mowat syndrome

scientific article published on December 1995

Microcephaly and early-onset nephrotic syndrome ?confusion in Galloway-Mowat syndrome

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Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

14 October 2017

Microcephaly and early-onset nephrotic syndrome--confusion in Galloway-Mowat syndrome (English)

1 reference

Europe PubMed Central

PubMed publication ID

14 October 2017

0 references

author name string

H Sano

1

1 reference

Europe PubMed Central

PubMed publication ID

14 October 2017

A Miyanoshita

2

1 reference

Europe PubMed Central

PubMed publication ID

14 October 2017

N Watanabe

3

1 reference

Europe PubMed Central

PubMed publication ID

14 October 2017

Y Koga

4

1 reference

Europe PubMed Central

PubMed publication ID

14 October 2017

Y Miyazawa

5

1 reference

Europe PubMed Central

PubMed publication ID

14 October 2017

Y Yamaguchi

6

1 reference

Europe PubMed Central

PubMed publication ID

14 October 2017

Y Fukushima

7

1 reference

Europe PubMed Central

PubMed publication ID

14 October 2017

N Itami

8

1 reference

Europe PubMed Central

PubMed publication ID

14 October 2017

publication date

1 December 1995

1 reference

Europe PubMed Central

PubMed publication ID

14 October 2017

Pediatric Nephrology

1 reference

Europe PubMed Central

PubMed publication ID

14 October 2017

9

1 reference

Europe PubMed Central

PubMed publication ID

14 October 2017

6

1 reference

Europe PubMed Central

PubMed publication ID

14 October 2017

711-714

1 reference

Europe PubMed Central

PubMed publication ID

14 October 2017

https://scigraph.springernature.com/pub.10.1007/bf00868718

0 references

Congenital microcephaly and infantile nephrotic syndrome--a case report

1 reference

https://pubmed.ncbi.nlm.nih.gov/8747110

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Microcephaly and congenital nephrotic syndrome owing to diffuse mesangial sclerosis: an autosomal recessive syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/8747110

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clinical quiz. Congenital nephrotic syndrome, microcephaly, brain malformations and diaphragmatic abnormality associated with histological features of diffuse mesangial sclerosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/8747110

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Congenital microcephaly with hiatus hernia and nephrotic syndrome in two sibs

1 reference

https://pubmed.ncbi.nlm.nih.gov/8747110

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[Familial microcephalies due to cerebral malformation. Anatomical and clinical study]

1 reference

https://pubmed.ncbi.nlm.nih.gov/8747110

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Focal segmental glomerulosclerosis associated with infantile spasms in five mentally retarded children: a morphological analysis on mesangiolysis

1 reference

https://pubmed.ncbi.nlm.nih.gov/8747110

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Kidney in Galloway-Mowat syndrome: clinical spectrum with description of pathology

1 reference

https://pubmed.ncbi.nlm.nih.gov/8747110

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Galloway-Mowat syndrome of abnormal gyral patterns and glomerulopathy

1 reference

https://pubmed.ncbi.nlm.nih.gov/8747110

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Congenital microcephaly, infantile spasms, psychomotor retardation, and nephrotic syndrome in two sibs

1 reference

https://pubmed.ncbi.nlm.nih.gov/8747110

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

1 reference

https://pubmed.ncbi.nlm.nih.gov/8747110

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[Congenital microcephaly with muscle hypotonia and nephrotic syndrome]

1 reference

https://pubmed.ncbi.nlm.nih.gov/8747110

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Pachygyria and congenital nephrosis disorder of migration and neuronal orientation

1 reference

https://pubmed.ncbi.nlm.nih.gov/8747110

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Congenital microcephaly, hiatus hernia and nephrotic syndrome: an autosomal recessive syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/8747110

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[Association of early-onset nephrotic syndrome and microcephaly. Apropos of 4 cases in 2 families]

1 reference

https://pubmed.ncbi.nlm.nih.gov/8747110

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00868718

1 reference

Europe PubMed Central

PubMed publication ID

14 October 2017

Dimensions Publication ID

0 references

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

14 October 2017

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