Results 91 to 100 of about 568 (137)

Targeting Metabolomics in Primary Hypertrophic Osteoarthropathy: Uncovering Novel Insights into Disease Pathogenesis.

J Clin Endocrinol Metab
Pang Q, Qi X, Chi Y, Jiajue R, Zhang L, Cui L, Wang O, Li M, Xing X, Jiang Y, Gong Y, Xia W.   +11 more
europepmc   +1 more source

Clinical and genetic characteristics of Chinese patients diagnosed with chronic enteropathy associated with SLCO2A1 gene. [PDF]

Orphanet J Rare Dis
Shang Q, Dai Y, Huang J, Liu W, Zhou W, Liu Y, Yang H, Wang Q, Li Y.   +8 more
europepmc   +1 more source

Pachydermoperiostosis Due to a Novel HPGD Splicing Site Mutation Masquerading as Acromegaly. [PDF]

JCEM Case Rep
Almalki M, Alghamdi B, Benito A, Alfares A, Alzahrani AS.   +4 more
europepmc   +1 more source

Bullous Mastocytosis: A Rare Variant of Diffuse Cutaneous Mastocytosis. [PDF]

Cureus
Almheiri SK, Pakran J, AlFalasi AA, El Bahtimi R.   +3 more
europepmc   +1 more source

Genotype-Phenotype Correlation Insights in a Rare Case Presenting with Multiple Osteodysplastic Syndromes. [PDF]

Genes (Basel)
Yapijakis C, Gintoni I, Chamakioti M, Koniari E, Papanikolaou E, Kassi E, Vlachakis D, Chrousos GP.   +7 more
europepmc   +1 more source

Mastocytosis in the Skin: Approach to Diagnosis, Evaluation, and Management in Adult and Pediatric Patients. [PDF]

Am J Clin Dermatol
Madigan LM, Boggs NA, Rets AV, Gru AA, Tashi T, Wada DA, Florell SR, Carter MC.   +7 more
europepmc   +1 more source

Hereditary α-Tryptasemia and Peripheral Blood <i>KIT</i> D816V Mutation in Patients with Pediatric Mastocytosis. [PDF]

Int J Mol Sci
Tockova O, Planinsek Rucigaj T, Ivancan S, Bidovec Stojkovic U, Rijavec M, Šelb J, Korošec P.   +6 more
europepmc   +1 more source

Etiology of pachydermia diffusa. Proposal of a hypothesis and afterward development.

Japanese Journal of Clinical Immunology, 1997
openaire   +2 more sources

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Hypertrophic Osteoarthropathy Without Pachydermia

American Journal of Diseases of Children, 1975
A 3-year-old boy had primary hypertrophic osteoarthropathy without pachydermia. This case is similar to several others previously described, and it could possibly represent a distinct nosological form of osteoarthropathy.
G, Bartolozzi, G, Bernini, M, Maggini
exaly   +3 more sources