Results 211 to 220 of about 5,264 (268)

Pulmonary Hyalinizing Granuloma with Radiological Cystic Lesion. [PDF]

open access: yesIntern Med
Yamakawa H   +3 more
europepmc   +1 more source

Molecular dynamics of the matrisome across sea anemone life history. [PDF]

open access: yesElife
Bergheim BG   +7 more
europepmc   +1 more source

Post-Mortem Detection and Visualization of Mimivirus Reactivation in Fatal Viral Pneumonia. [PDF]

open access: yesViruses
Khachatryan P   +17 more
europepmc   +1 more source

Juvenile hyaline fibromatosis

Journal of the American Academy of Dermatology, 1987
The literature recording cases of the rare juvenile hyaline fibromatosis is reviewed. Gingival enlargement is a regular feature of this entity. A case report and treatment of the gingival lesions are described, and the differential diagnosis and prognosis are discussed.
J G, Camarasa, A, Moreno
  +7 more sources

Juvenile non‐hyaline fibromatosis: juvenile hyaline fibromatosis without prominent hyaline changes

Journal of Cutaneous Pathology, 2005
Abstract:  Juvenile hyaline fibromatosis (JHF) is a rare autosomal recessive disease of the connective tissue. It is characterized by papulonodular skin lesions, soft tissue masses, gingival hypertrophy, osteolytic bone lesions and flexion contractures of the large joints.
Rana Yavuzer, Anadolu   +3 more
openaire   +2 more sources

Histochemistry of sarcoidotic-hyaline

Pneumonologie Pneumonology, 1976
On account of its weaker reactions for tryptophan, tyrosine, proteolipids, and lipoproteins, sarcoidotic-hyaline (Sa. Hy.) is immediately distinguishable from caseosis. However, protein histochemistry fails to differentiate Sa. Hy. from normal (fixed and insoluble postfixed) and pericaseous collagen. Evidence of this is provided by the present study on
G, Barbolini, S, Battaglia
openaire   +2 more sources

Juvenile hyaline Fibromatose

Der Hautarzt, 1997
Juvenile hyaline fibromatosis is a rare autosomal recessive connective tissue disease first described in 1873 by Murray. Major diagnostic criteria are multiple cutaneous tumors and gingival hypertrophy; minor criteria include contractures, osteolytic lesions and a positive family history.
M, Schaller   +3 more
openaire   +2 more sources

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