(Q37147814)

18 August 2017

Hutchinson-Gilford progeria syndrome: oral and craniofacial phenotypes (English)

1 reference

18 August 2017

1 reference

D L Domingo

1

1 reference

18 August 2017

M I Trujillo

2

1 reference

18 August 2017

S E Council

3

1 reference

18 August 2017

M A Merideth

4

1 reference

18 August 2017

L B Gordon

5

1 reference

18 August 2017

T Wu

6

1 reference

18 August 2017

W J Introne

7

1 reference

18 August 2017

W A Gahl

8

1 reference

18 August 2017

T C Hart

9

1 reference

18 August 2017

19 February 2009

1 reference

18 August 2017

1 reference

18 August 2017

15

1 reference

18 August 2017

3

1 reference

18 August 2017

187-195

1 reference

Phenotype and course of Hutchinson-Gilford progeria syndrome

18 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2664390

The mutant form of lamin A that causes Hutchinson-Gilford progeria is a biomarker of cellular aging in human skin

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2664390

Dermal fibroblasts in Hutchinson-Gilford progeria syndrome with the lamin A G608G mutation have dysmorphic nuclei and are hypersensitive to heat stress

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2664390

Ankyloglossia: a morphofunctional investigation in children

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2664390

Genetic modulation of senescent phenotypes in Homo sapiens

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2664390

Heterozygosity for Lmna deficiency eliminates the progeria-like phenotypes in Zmpste24-deficient mice

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2664390

Hutchinson-Gilford progeria syndrome

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2664390

Accumulation of mutant lamin A causes progressive changes in nuclear architecture in Hutchinson-Gilford progeria syndrome

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2664390

The interdisciplinary management of hypodontia: background and role of paediatric dentistry.

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2664390

Hypodontia: etiology, clinical features, and management.

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2664390

Hutchinson-Guilford progeria syndrome

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2664390

Dental development, dental age and tooth counts

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2664390

Progeria in a pediatric dental patient: literature review and case report

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2664390

Progeria: report of a case and review of the literature

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2664390

Progeria: clinical considerations of an isolated case

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2664390

Supernumerary and congenitally absent teeth: a literature review

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2664390

Restrictive dermopathy: report and review

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2664390

Disease progression in Hutchinson-Gilford progeria syndrome: impact on growth and development.

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2664390

Hutchinson-Gilford progeria syndrome: review of the phenotype.

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2664390

Is the mandible intrinsically different in Apert and Crouzon syndromes?

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2664390

Management of severe partial hypodontia: case report

3 September 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19236595

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

The use of overdentures in the management of severe hypodontia associated with microdontia: a case report

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19236595

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Werner syndrome and mutations of the WRN and LMNA genes in France

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19236595

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1111/J.1601-0825.2009.01521.X

1 reference

18 August 2017

1 reference

18 August 2017

PubMed publication ID

19236595

1 reference