Results 171 to 180 of about 45,305 (223)

Dermatological Manifestations of Amyloid Light-Chain (AL) Amyloidosis: A Case Report Highlighting Early Diagnosis and Treatment. [PDF]

Cureus
Gill SS, Kamboj T.
europepmc   +1 more source

Transaldolase Deficiency in a Saudi Girl: Identification of a Novel Homozygous TALDO1 Variant. [PDF]

Cureus
Asiri K, Rayees S, Alasmari BG.
europepmc   +1 more source

Neonatal-onset familial hemophagocytic lymphohistiocytosis: a case report with genetic confirmation of PRF1 mutations. [PDF]

Front Genet
Lyu X, Wei P, Zhu L, Zhang W.
europepmc   +1 more source

Crimean-Congo hemorrhagic fever: serum neopterin levels and their relationship with clinical course. [PDF]

Rev Assoc Med Bras (1992)
Usanmaz M.
europepmc   +1 more source

Bone-in-bone and sandwich vertebrae in a 6-month-old infant with genetically confirmed fatal osteopetrosis: A case report. [PDF]

Medicine (Baltimore)
Hou F, Zhang J.
europepmc   +1 more source

A Rare Case of Hemophagocytic Lymphohistiocytosis Triggered by Intravesical Bacillus Calmette-Guérin (BCG) for Bladder Cancer. [PDF]

Cureus
Nakayama M, Yanagihara T, Fujimoto M, Kushima N, Okabe Y, Aoki M, Koga K, Yokoyama K, Sakaki Y, Ikeda T, Hamada N, Hamasaki M, Fujita M.   +12 more
europepmc   +1 more source

Schistosomiasis, endless endemicity since the ancient Egyptians. [PDF]

BMC Infect Dis
Ramadan A, Sabry F, Gaheen AM, Rabat AE, Mohamed EM, Helal A, Eissa M, Farag SA, Badra GA, El Fayoumy M.   +9 more
europepmc   +1 more source

Pediatric Sneddon syndrome presenting with early-onset liver fibrosis: a rare case report. [PDF]

Oxf Med Case Reports
Awad QN, Makhlouf TZ, Zhour MF, Bannoura S, Abu Hussein W.   +4 more
europepmc   +1 more source

Hermansky-Pudlak syndrome-rare type 10 with AP3D1 mutation. [PDF]

Oxf Med Case Reports
Balaraddi V, Nawlakhe K, K S, Bandiya P.
europepmc   +1 more source