Results 111 to 120 of about 635 (170)
Pachydermoperiostosis Due to a Novel HPGD Splicing Site Mutation Masquerading as Acromegaly. [PDF]
Almalki M +4 more
europepmc +1 more source
Bullous Mastocytosis: A Rare Variant of Diffuse Cutaneous Mastocytosis. [PDF]
Almheiri SK +3 more
europepmc +1 more source
Mastocytosis in the Skin: Approach to Diagnosis, Evaluation, and Management in Adult and Pediatric Patients. [PDF]
Madigan LM +7 more
europepmc +1 more source
Hereditary α-Tryptasemia and Peripheral Blood <i>KIT</i> D816V Mutation in Patients with Pediatric Mastocytosis. [PDF]
Tockova O +6 more
europepmc +1 more source
Molecular basis of prostaglandin E<sub>2</sub> reuptake by organic anion transporter PGT. [PDF]
Zhu Z +8 more
europepmc +1 more source
Olmsted Syndrome in a 12-year-old Filipino Male: A Case Report and Future Directions. [PDF]
Pandapatan AT, Tan CJ, Tan JAS.
europepmc +1 more source
Treatment of pachydermoperiostosis pachydermia with botulinum toxin type A
Pachydermoperiostosis (PDP) is a rare hereditary disorder characterized by digital clubbing, periostosis, and pachydermia. Pachydermia results in leonine facies, a major cause of cosmetic and functional morbidity in these patients. Its treatment is usually surgical.
Samer Ghosn +4 more
openalex +3 more sources

