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Annals of Neurology, ISSN 0364-5134, 05/2019, Volume 85, Issue 5, pp. 740 - 751
Journal Article
Pediatric Neurology, ISSN 0887-8994, 07/2019, Volume 96, pp. 70 - 73
Enterovirus-A71 causes outbreaks of brainstem encephalitis, ranging from self-limited disease to acute flaccid paralysis. The aim of this study was to assess... 
EV-A71 | Biomarkers | Enterovirus | Neopterin | Brainstem encephalitis | ACTIVATION | PEDIATRICS | CLINICAL NEUROLOGY | Medical research | Encephalitis | Pediatric intensive care | Medicine, Experimental | Brain damage | Children | Paralysis | Health aspects | Pediatric neurology
Journal Article
The Journal of Maternal-Fetal & Neonatal Medicine, ISSN 1476-7058, 03/2020, Volume 33, Issue 6, pp. 1024 - 1026
Neonatal hemochromatosis (NH) has been defined as neonatal liver disorder accompanied by extrahepatic siderosis, and gestational alloimmune liver disease... 
Exchange transfusion | neonatal hemochromatosis | tyrosine | gestational alloimmune disease | methionine | intravenous immunoglobulin | OBSTETRICS & GYNECOLOGY
Journal Article
The Pediatric Infectious Disease Journal, ISSN 0891-3668, 12/2016, Volume 35, Issue 12, pp. 1366 - 1368
Human parechovirus-3 has been associated with severe clinical manifestations in infants, such as sepsis-like illness and meningoencephalitis. Nevertheless, the... 
Hemophagocytic lymphohistiocytosis | Hyperferritinemia | Human parechovirus-3 | INFECTIOUS DISEASES | human parechovirus-3 | INFANTS | hemophagocytic lymphohistiocytosis | PEDIATRICS | IMMUNOLOGY | hyperferritinemia | Iron Metabolism Disorders | Parechovirus | Humans | Twins, Dizygotic | Female | Infant | Male | Picornaviridae Infections | Lymphohistiocytosis, Hemophagocytic
Journal Article
International Journal of Medical Sciences, ISSN 1449-1907, 2019, Volume 16, Issue 2, pp. 231 - 240
Colorectal cancer (CRC) is one of leading cause of mortality in western countries and novel treatment strategies are required. The medicinal application of... 
Colon cancer | Proliferation | Fugal extracts | Invasion | CADHERIN | MATRIX METALLOPROTEINASES | APOPTOSIS | MEDICINE, GENERAL & INTERNAL | invasion | proliferation | ROLES | D-FRACTION | CORIOLUS-VERSICOLOR | fugal extracts | PLASTICITY
Journal Article
Journal of Pediatric Endocrinology and Metabolism, ISSN 0334-018X, 05/2017, Volume 30, Issue 5, pp. 597 - 601
Journal Article
Scientific Reports, ISSN 2045-2322, 12/2018, Volume 8, Issue 1, pp. 3466 - 10
Journal Article
Journal Article
American Journal of Medical Genetics Part A, ISSN 1552-4825, 01/2020, Volume 182, Issue 1, pp. 20 - 24
Okur‐Chung neurodevelopmental syndrome (OCNS, MIM#617062) is a rare autosomal dominant syndrome related to CSNK2A1 mutations. It is characterized by... 
CSNK2A1 | Okur‐Chung neurodevelopmental syndrome | pituitary gland duplication | Vertebrae | Magnetic resonance imaging | Pituitary | Olfactory bulb | Mutation | Neurodevelopmental disorders | Mental retardation
Journal Article
El Pais, 07/2015
Newspaper Article
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