(Q36324132)

English

Light microscopic examination of scalp hair samples as an aid in the diagnosis of paediatric disorders: retrospective review of more than 300 cases from a single centre

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

13 August 2017

Light microscopic examination of scalp hair samples as an aid in the diagnosis of paediatric disorders: retrospective review of more than 300 cases from a single centre (English)

1 reference

Europe PubMed Central

PMC publication ID

13 August 2017

author name string

Smith VV

1

1 reference

Europe PubMed Central

PMC publication ID

13 August 2017

Anderson G

2

1 reference

Europe PubMed Central

PMC publication ID

13 August 2017

Malone M

3

1 reference

Europe PubMed Central

PMC publication ID

13 August 2017

Sebire NJ

4

1 reference

Europe PubMed Central

PMC publication ID

13 August 2017

language of work or name

0 references

publication date

1 December 2005

1 reference

Europe PubMed Central

PMC publication ID

13 August 2017

Journal of Clinical Pathology

1 reference

Europe PubMed Central

PMC publication ID

13 August 2017

58

1 reference

Europe PubMed Central

PMC publication ID

13 August 2017

12

1 reference

Europe PubMed Central

PMC publication ID

13 August 2017

1294-1298

1 reference

Europe PubMed Central

PMC publication ID

13 August 2017

Characterization of tiger-tail banding and hair shaft abnormalities in trichothiodystrophy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1770794

30 September 2017

Spink5-deficient mice mimic Netherton syndrome through degradation of desmoglein 1 by epidermal protease hyperactivity

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1770794

30 September 2017

"Curly" wood and tiger tails: an explanation for light and dark banding with polarization in trichothiodystrophy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1770794

30 September 2017

Griscelli syndrome restricted to hypopigmentation results from a melanophilin defect (GS3) or a MYO5A F-exon deletion (GS1)

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1770794

30 September 2017

Chediak-Higashi syndrome: a clinical and molecular view of a rare lysosomal storage disorder

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1770794

30 September 2017

Evidence that Griscelli syndrome with neurological involvement is caused by mutations in RAB27A, not MYO5A

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1770794

30 September 2017

Netherton syndrome: disease expression and spectrum of SPINK5 mutations in 21 families

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1770794

30 September 2017

Uncombable hair (cheveux incoiffables, pili trianguli et canaliculi) syndrome: brief review and role of scanning electron microscopy in diagnosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1770794

30 September 2017

Two genes are responsible for Griscelli syndrome at the same 15q21 locus.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1770794

30 September 2017

Structural abnormalities of the hair shaft

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1770794

30 September 2017

Loose anagen hair

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1770794

29 June 2018

Griscelli disease: genotype-phenotype correlation in an array of clinical heterogeneity

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1770794

22 September 2018

Kinky hair disease. I. Clinical and pathological features.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1770794

22 September 2018

Netherton's syndrome: increased likelihood of diagnosis by examining eyebrow hairs

1 reference

https://pubmed.ncbi.nlm.nih.gov/16311350

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An optical study of human hair colour in normal and abnormal conditions

1 reference

https://pubmed.ncbi.nlm.nih.gov/16311350

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Pathogenesis in trichorrhexis invaginata (bamboo hair)

1 reference

https://pubmed.ncbi.nlm.nih.gov/16311350

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Rapp-Hodgkin syndrome: observations on ten cases and characteristic hair changes (pili canaliculi)

1 reference

https://pubmed.ncbi.nlm.nih.gov/16311350

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Loose anagen hair of childhood: the phenomenon of easily pluckable hair

1 reference

https://pubmed.ncbi.nlm.nih.gov/16311350

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Autosomal recessive neurodegenerative disorder with trichorrhexis invaginata and ectodermal dysplasia

1 reference

https://pubmed.ncbi.nlm.nih.gov/16311350

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Uncombable hair, retinal pigmentary distrophy, dental anomalies, and brachydactyly: Report of a new patient with additional findings

1 reference

https://pubmed.ncbi.nlm.nih.gov/16311350

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Apparent genotype-phenotype correlation in childhood, adolescent, and adult Chediak-Higashi syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/16311350

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1136/JCP.2005.027581

1 reference

Europe PubMed Central

PMC publication ID

13 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

13 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

13 August 2017

ResearchGate publication ID

0 references

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