Pyknodysostosis: visceral manifestations and simian crease (Q44911218)

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Language	Label	Description	Also known as
English	Pyknodysostosis: visceral manifestations and simian crease	scientific article

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

7 December 2017

Pyknodysostosis: visceral manifestations and simian crease (English)

1 reference

Europe PubMed Central

PubMed publication ID

7 December 2017

author name string

Arvind Rup Singh

1

1 reference

Europe PubMed Central

PubMed publication ID

7 December 2017

Anupam Kaur

2

1 reference

Europe PubMed Central

PubMed publication ID

7 December 2017

Nand Kishore Anand

3

1 reference

Europe PubMed Central

PubMed publication ID

7 December 2017

Jai Rup Singh

4

1 reference

Europe PubMed Central

PubMed publication ID

7 December 2017

publication date

1 May 2004

1 reference

Europe PubMed Central

PubMed publication ID

7 December 2017

Indian Journal of Pediatrics

1 reference

Europe PubMed Central

PubMed publication ID

7 December 2017

71

1 reference

Europe PubMed Central

PubMed publication ID

7 December 2017

5

1 reference

Europe PubMed Central

PubMed publication ID

7 December 2017

453-455

1 reference

Europe PubMed Central

PubMed publication ID

7 December 2017

https://scigraph.springernature.com/pub.10.1007/bf02725641

0 references

Pycnodysostosis. Clinical and genetic considerations

1 reference

https://api.crossref.org/works/10.1007%2FBF02725641

21 January 2018

Pycnodysostosis, a lysosomal disease caused by cathepsin K deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/15163881

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Defective growth hormone secretion in children with pycnodysostosis and improved linear growth after growth hormone treatment

1 reference

https://pubmed.ncbi.nlm.nih.gov/15163881

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mouse cathepsin K: cDNA cloning and predominant expression of the gene in osteoclasts, and in some hypertrophying chondrocytes during mouse development

1 reference

https://pubmed.ncbi.nlm.nih.gov/15163881

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Pycnodysostosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/15163881

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Pyknodysostosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/15163881

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Pycnodysostosis associated with delayed and ectopic eruption of permanent teeth

1 reference

https://pubmed.ncbi.nlm.nih.gov/15163881

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Osteopetrosis acro-osteolytica. A syndrome of osteopetrosis, acro-osteolysis and open sutures of the skull

1 reference

https://pubmed.ncbi.nlm.nih.gov/15163881

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Determination of bone markers in pycnodysostosis: effects of cathepsin K deficiency on bone matrix degradation.

1 reference

https://pubmed.ncbi.nlm.nih.gov/15163881

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Pycnodysostosis: refined linkage and radiation hybrid analyses reduce the critical region to 2 cM at 1q21 and map two candidate genes

1 reference

https://pubmed.ncbi.nlm.nih.gov/15163881

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Pycnodysostosis. Orthopedic aspects with a description of 14 new cases

1 reference

https://pubmed.ncbi.nlm.nih.gov/15163881

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Pycnodysostosis: A Variant Form with Visceral Manifestations

1 reference

https://pubmed.ncbi.nlm.nih.gov/15163881

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Pyknodysostosis: extreme cause of sleep apnea

1 reference

https://pubmed.ncbi.nlm.nih.gov/15163881

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Pycnodysostosis with visceral manifestation and rickets

1 reference

https://pubmed.ncbi.nlm.nih.gov/15163881

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Human Gene Mutation Database (HGMD): 2003 update

1 reference

https://pubmed.ncbi.nlm.nih.gov/15163881

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Pycnodysostosis: clinical, radiologic, and endocrine evaluation and linear growth after growth hormone therapy

1 reference

https://pubmed.ncbi.nlm.nih.gov/15163881

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF02725641

1 reference

Europe PubMed Central

PubMed publication ID

7 December 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

7 December 2017

ResearchGate publication ID

0 references

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