Results 101 to 110 of about 32,645 (198)

Rash and hepatosplenomegaly in a newborn

JMM Case Reports, 2017
Kitt, Eimear, May, Rebecca M., Steenhoff, Andrew P.   +2 more
openaire   +2 more sources

Autosomal recessive human CTLA-4 deficiency with autoimmune infiltration. [PDF]

J Hum Immun
Su HC.
europepmc   +1 more source

Correction: TAFRO syndrome requiring combined IL 6 and IL 1 inhibition: a case report. [PDF]

Front Immunol
Frontiers Production Office.
europepmc   +1 more source

Early Diagnosis of Nieman-Pick Disease Type C and Rapid Response of Gelastic Cataplexy to Treatment With N-Acetyl-L-Leucine: A Case Report. [PDF]

Am J Case Rep
Rojnueangnit K, Puttamanee S, Intarakhao S, Khusiwilai K.   +3 more
europepmc   +1 more source

Cooccurrence of myelodysplastic neoplasm and myeloid sarcoma with background mediastinal germ cell tumor: an autopsy case. [PDF]

J Clin Exp Hematop
Kaimi Y, Haga T, Yamaguchi Y, Sudo K, Yonemori K, Yatabe Y.   +5 more
europepmc   +1 more source

Hidden Behind Ascites: An Atypical Pediatric Presentation of T-Cell Acute Lymphoblastic Leukemia-A Case Report. [PDF]

Clin Case Rep
Shaikh K, Anas Z, Rajput S, Zaib A, Saleem A, Haque MA.   +5 more
europepmc   +1 more source

A Comprehensive Literature Review and Case Report of Severe Lymphoproliferative Disease Secondary to <i>CD137</i> Deficiency. [PDF]

J Clin Med
Algrafi AS, Alwasaidi T, Albalawi M, Alzahrani M, Almutairi S, Osman H.   +5 more
europepmc   +1 more source

Aggressive Systemic Mastocytosis Presenting as Diffuse Osteoblastic Bone Disease: A Diagnostic Pitfall Mimicking Metastatic Cancer. [PDF]

Eur J Case Rep Intern Med
Melício A, Gonçalves HD, Dias M, Vasconcelos-Teixeira S, Madeira Lopes J.   +4 more
europepmc   +1 more source

Expanding the scope of PI3K-δ inhibition: Leniolisib treatment in PRKCD deficiency. [PDF]

J Hum Immun
Lodi L, Guarnieri V, Peri M, Baronio M, Ricci S, Canessa C, Lippi F, Voarino M, Calistri E, Pisano L, Perrone A, Fenu G, Indolfi G, Lougaris V, Marsh RA, Azzari C.   +15 more
europepmc   +1 more source

Repurposing Gaucher disease therapy for Saposin C deficiency: Proof-of-concept with eliglustat.

Mol Genet Metab
Minea C, Deegan PB.
europepmc   +1 more source