Results 161 to 170 of about 37,115 (234)

Isolated Non-Progressive Hemidystonia in a Patient Homozygous for H63D Variant of Hereditary Hemochromatosis: A Case Report and Systematic Literature Review of Movement Disorders in Hereditary Hemochromatosis. [PDF]

Diagnostics (Basel)
Kalampokini S, Plaitakis A, Spanaki C, Xiromerisiou G.   +3 more
europepmc   +1 more source

Editorial: Differential diagnosis of erythrocytosis and analysis of their clinical utility. [PDF]

Front Med (Lausanne)
Lekovic D, Sobas M, Lucijanic M.
europepmc   +1 more source

Persistent Beetroot Colored Urine in a Three-Year-Old Child: A Case Report. [PDF]

Clin Case Rep
Harper P, Törnhage CJ, Sardh E.
europepmc   +1 more source

β-thalassemia trait and iron overload: is it time to consider oral iron chelators? Comment on: "A case series of patients with β-thalassemia trait and iron overload: from multifactorial hepcidin suppression to treatment with mini-phlebotomies". [PDF]

Haematologica
Piperno A, Mariani R.
europepmc   +1 more source

Hair Loss and Bronze Discoloration of the Skin in Lupus Erythematosus. [PDF]

Dtsch Arztebl Int
Dibaj P, Gärtner J.
europepmc   +1 more source

Mean Corpuscular Volume in <i>HFE</i> p.C282Y/p.H63D Compound Heterozygotes With High Iron Phenotypes: Clinical and Laboratory Associations. [PDF]

J Hematol
Barton JC, Barton JC, Acton RT.
europepmc   +1 more source

Reference diagnosis and treatment process of juvenile hemochromatosis patients. [PDF]

World J Clin Cases
He YC, Wang NX, Zhong T.
europepmc   +1 more source

HFE mutations in patients with iron overload in Santa Catarina: a cross-sectional study. [PDF]

Sao Paulo Med J
Pagliosa CM, Franco VKB, Matias TS, Dias BV, Hoepers ATC.   +4 more
europepmc   +1 more source

Not All Hereditary Iron Overload Is Hemochromatosis: A Case of Hereditary Xerocytosis Unmasked by Blood Smear Morphology. [PDF]

Am J Hematol
Molina-Arrebola MA, Bain BJ.
europepmc   +1 more source