Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

[A rare genotypic bone disease: "pycnodysostosis" (a new case in a 60-year-old man)].

Revue du rhumatisme et des maladies osteo-articulaires - 1 Jan 2000

Memin Y, Hiltenbrand C, Giudicelli C, Papillaud J

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Dwarfism
Share to Genotype
Share to Heart Failure
Share to Osteopetrosis

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Radiography

Source

Identifiers

PMID: 5507197

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

[A rare genotypic bone disease: "pycnodysostosis" (a new case in a 60-year-old man)].PMID 5507197Read ↗

[Pycnodysostosis, a case report].Semantic proximity Read ↗

Pycnodysostosis- A Rare Diagnosis Not to MissSemantic proximity Read ↗

[Proteus syndrome: contribution to its clinical delineation].Semantic proximity Read ↗

Pycnodysostosis: mutation spectrum in five unrelated Indian children.Semantic proximity Read ↗

[Paget's disease of bone associated with ZNF687 gene mutation: report of a case].Semantic proximity Read ↗

[Oral-facial-digital syndrome type II: clinical case and differential diagnosis].Semantic proximity Read ↗

[A case of autosomal recessive hypomyelinating leukodystrophy without GJA12 mutation presenting a novel phenotype].Semantic proximity Read ↗

Clinical and genetic characterization of three Russian patients with pycnodysostosis due to pathogenic variants in the CTSK gene.Semantic proximity Read ↗

[The POEMS syndrome, apropos of 2 cases and review of the literature].Semantic proximity Read ↗

[Pelizaeus-Merzbacher-caused diseases in Connexin 46 mutation: a rare form of leukodystrophy].Semantic proximity Read ↗

Case of genochondromatosis type I in an 8-year-old boy.Semantic proximity Read ↗

Spontaneous Atlas Fracture in a Patient with Pycnodysostosis and Mandibular Osteomyelitis: A Case ReportSemantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.