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Medical Journal of Bakirkoy, ISSN 1305-9319, 2017, Volume 13, Issue 2, pp. 107 - 109
Journal Article
Hepatosplenic Schistosomiasis in Field-based Studies: a Combined Clinical and Sonographic Definition, 12/2001
A combined clinical and sonographic classification of hepatosplenic schistosomiasis mansoni to be used in field-based studies is proposed herein. Seven hundred... 
schistosomiasis, ultrasound, hepatosplenomegaly, splenomegaly, morbidity
Journal
Journal of Clinical and Diagnostic Research, ISSN 2249-782X, 01/2018, Volume 12, Issue 1, pp. EC09 - EC11
Journal Article
Journal of Clinical and Diagnostic Research, ISSN 2249-782X, 07/2017, Volume 11, Issue 7, pp. XD12 - XD13
Polyneuropathy, Organomegaly, Endocrinopathy, M protein and Skin changes (POEMS) syndrome is rare plasma cell dyscrasia with multisystem involvement. The name... 
Hepatosplenomegaly | Protein electrophoresis | Multiple myeloma | Oncology Section
Journal Article
Journal of Clinical and Diagnostic Research, ISSN 2249-782X, 05/2017, Volume 11, Issue 5, pp. SJ01 - SJ02
Journal Article
CHIRURG, ISSN 0009-4722, 10/2019, Volume 90, Issue 10, pp. 833 - 837
Visceral leishmaniasis is a worldwide distributed infectious zoonotic disease caused by protozoan pathogens of the genus Leishmania which are transmitted by... 
Surgical aspects | SURGERY | Opportunistic infection | Immunosuppression | Hepatosplenomegaly | CANINE LEISHMANIASIS | PATIENT | SPLENECTOMY | AREAS | Epidemiology
Journal Article
Experimental Parasitology, ISSN 0014-4894, 06/2019, Volume 201, pp. 49 - 56
Trypanosoma congolense is an important pathogen that wreaks havoc in the livestock industry of the African continent. This study evaluated the in vivo... 
Anaemia | Hepatosplenomegaly | Geranylacetone | Molecular docking | Sialidase | Trypanosoma congolense | DOCKING | ESSENTIAL OIL | LEAVES | FEATURES | COULD | INFECTION | INHIBITORS | DERIVATIVES | PARASITOLOGY | BLOOD-CELLS
Journal Article
Clinical Nuclear Medicine, ISSN 0363-9762, 04/2018, Volume 43, Issue 4, pp. e125 - e126
ABSTRACTIntravascular lymphoma (IVL) is a rare subtype of diffuse large B-cell lymphoma characterized by a clonal proliferation of lymphocytes restricted to... 
hepatosplenomegaly | intravascular lymphoma | hemophagocytic syndrome | PATIENT | ASIAN VARIANT | RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING
Journal Article
Turkish Journal of Hematology, ISSN 1300-7777, 2014, Volume 31, Issue 3, pp. 307 - 308
Journal Article
Medicina Clinica, ISSN 0025-7753, 09/2011, Volume 137, Issue 1, pp. 43 - 45
We report two cases of type 1 Gaucher's disease in childhood and their outcomes after 9 years of enzyme replacement therapy. The first case concerns a... 
Thrombocytopenia | Puberty | Hepatosplenomegaly | Growth | Childhood
Journal Article
Journal of Clinical and Diagnostic Research, ISSN 2249-782X, 07/2017, Volume 11, Issue 7, pp. ED24 - ED26
Myeloid sarcoma is an extramedullary manifestation of Acute Myeloid Leukaemia and sometimes is the only indicator of the disease. The incidence varies between... 
Hepatosplenomegaly | Lymphocytes | Chloroma | Pathology Section
Journal Article
Pan African Medical Journal, ISSN 1937-8688, 2015, Volume 20
Journal Article
Journal of Infection and Chemotherapy, ISSN 1341-321X, 06/2019, Volume 25, Issue 6, pp. 431 - 436
Infectious mononucleosis (IM) is a common viral infection that typically causes fever, pharyngitis, and lymphadenopathy in young patients. The Epstein-Barr... 
Lymphadenopathy | Tonsillar white coat | Hepatosplenomegaly | Infectious mononucleosis-like syndrome | Atypical lymphocytosis | INFECTIOUS DISEASES | PHARMACOLOGY & PHARMACY | FEATURES
Journal Article
Journal de Gynecologie Obstetrique et Biologie de la Reproduction, ISSN 0368-2315, 12/2010, Volume 39, Issue 8, pp. 667 - 671
Risk for leukemic conditions increases in individuals with Down syndrome. We report a third trimester antenatal diagnosis of leukemia in a Down syndrome fetus.... 
Hepatosplenomegaly | Leukemia | Down syndrome
Journal Article
Case reports in gastroenterology, ISSN 1662-0631, 09/2019, Volume 13, Issue 3, pp. 498 - 507
Lysosomal acid lipase deficiency (LALD) is a rare genetic disease characterized by the accumulation of cholesteryl esters and triglycerides in many organs,... 
hepatosplenomegaly | sebelipase alfa | lysosomal acid lipase deficiency | fatty liver disease
Journal Article
Journal, Indian Academy of Clinical Medicine, ISSN 0972-3560, 10/2017, Volume 18, Issue 4, pp. 245 - 247
Journal Article
Pediatria Polska, ISSN 0031-3939, 03/2012, Volume 87, Issue 2, pp. 192 - 197
Malignant infantile osteopetrosis is a rare inherited via the autosomal recessive pattern metabolic disease caused by osteoclast failure leading to failed bone... 
osteopetrosis | children | hepatosplenomegaly | pancytopenia
Journal Article
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