(Q41935901)

14 October 2017

title

Neuropathological homology in true Galloway-Mowat syndrome (English)

1 reference

14 October 2017

Julia Keith

1

1 reference

14 October 2017

Victoria A Fabian

2

1 reference

14 October 2017

Peter Walsh

3

1 reference

14 October 2017

Raja Sinniah

4

1 reference

14 October 2017

Yves Robitaille

5

1 reference

14 October 2017

publication date

13 January 2011

1 reference

Journal of Child Neurology

14 October 2017

published in

1 reference

14 October 2017

volume

26

1 reference

14 October 2017

issue

4

1 reference

14 October 2017

page(s)

510-517

1 reference

Congenital microcephaly with hiatus hernia and nephrotic syndrome in two sibs

14 October 2017

cites work

1 reference

https://api.crossref.org/works/10.1177%2F0883073810383982

Pachygyria and congenital nephrosis disorder of migration and neuronal orientation

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073810383982

Nephrosis and disturbances of neuronal migration in male siblings--a new hereditary disorder?

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073810383982

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073810383982

Galloway-Mowat syndrome of abnormal gyral patterns and glomerulopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073810383982

Further case of Galloway-Mowat syndrome of abnormal gyral patterns and glomerulopathy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073810383982

A case of early myoclonic encephalopathy with the congenital nephrotic syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073810383982

Galloway-Mowat syndrome: a glomerular basement membrane disorder?

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073810383982

Recurrence of Galloway Mowat syndrome and associated prenatal imaging findings.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073810383982

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073810383982

Congenital microcephaly and infantile nephrotic syndrome--a case report

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073810383982

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073810383982

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073810383982

Galloway-Mowat syndrome in Taiwan

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073810383982

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073810383982

Diagnostic dilemmas in four infants with nephrotic syndrome, microcephaly and severe developmental delay

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073810383982

Podocyte proteins in Galloway-Mowat syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073810383982

Another autosomal recessive form of focal glomerulosclerosis with neurological findings

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073810383982

Collapsing glomerulopathy in Galloway-Mowat syndrome: a case report and review of the literature

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073810383982

Late-onset nephrotic syndrome and severe cerebellar atrophy in Galloway-Mowat syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073810383982

Microcephaly, cerebellar atrophy, and focal segmental glomerulosclerosis in two brothers: a possible mild form of Galloway-Mowat syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073810383982

Analysis of genes encoding laminin beta2 and related proteins in patients with Galloway-Mowat syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073810383982

Absence of the cerebellar granular layer, mental retardation, tapetoretinal degeneration and progressive glomerulopathy: an autosomal recessive oculo-renal-cerebellar syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073810383982

21 January 2018

Identifiers

DOI

10.1177/0883073810383982

1 reference

14 October 2017

1 reference