Related references
Note: Only part of the references are listed.Case Report: Epstein-Barr Virus Encephalitis Complicated With Brain Stem Hemorrhage in an Immune-Competent Adult
Lingtong Huang et al.
FRONTIERS IN IMMUNOLOGY (2021)
Thrombotic microangiopathy in aHUS and beyond: clinical clues from complement genetics
Fadi Fakhouri et al.
NATURE REVIEWS NEPHROLOGY (2021)
Quantitative analysis of the natural history of prolidase deficiency: description of 17 families and systematic review of published cases
Francis Rossignol et al.
GENETICS IN MEDICINE (2021)
A guide to interrogating immunometabolism
Kelsey Voss et al.
NATURE REVIEWS IMMUNOLOGY (2021)
Type IV Glycogen Storage Disease Associated With Hemophagocytic Lymphohistiocytosis: A Case Report
Ang Wei et al.
JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY (2020)
Propionic acidemia: an extremely rare cause of hemophagocytic lymphohistiocytosis in an infant
Sultan Aydin Koker et al.
ARCHIVOS ARGENTINOS DE PEDIATRIA (2020)
Hemophagocytic Lymphohystiocytosis Associated With Type Ia Glycogen Storage Disease
Yeter Duzenli Kar et al.
JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY (2019)
National survey of Japanese patients with mevalonate kinase deficiency reveals distinctive genetic and clinical characteristics
Takayuki Tanaka et al.
MODERN RHEUMATOLOGY (2019)
ETF-QO Mutants Uncoupled Fatty Acid β-Oxidation and Mitochondrial Bioenergetics Leading to Lipid Pathology
Suphannee Chokchaiwong et al.
CELLS (2019)
Hermansky-Pudlak syndrome type II and lethal hemophagocytic lymphohistiocytosis: Case description and review of the literature
Fabiola Dell'Acqua et al.
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY-IN PRACTICE (2019)
Deficiency of perforin and hCNT1, a novel inborn error of pyrimidine metabolism, associated with a rapidly developing lethal phenotype due to multi-organ failure
Sandra Perez-Torras et al.
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE (2019)
Metabolism as a guiding force for immunity
Jonathan Jung et al.
NATURE CELL BIOLOGY (2019)
Update on Lysinuric Protein Intolerance, a Multi-faceted Disease Retrospective cohort analysis from birth to adulthood
Wladimir Mauhin et al.
ORPHANET JOURNAL OF RARE DISEASES (2017)
An Unusual Case of LCHAD Deficiency Presenting With a Clinical Picture of Hemophagocytic Lymphohistiocytosis: Secondary HLH or Coincidence?
Sahin Erdol et al.
JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY (2016)
Hemophagocytic lymphohistiocytosis triggered by Gaucher disease in a preterm neonate
Simone Schueller et al.
PEDIATRIC HEMATOLOGY AND ONCOLOGY (2016)
Wolman disease associated with hemophagocytic lymphohistiocytosis: attempts for an explanation
Roberta Taurisano et al.
EUROPEAN JOURNAL OF PEDIATRICS (2014)
Clinical features and ETFDH mutation spectrum in a cohort of 90 Chinese patients with late-onset multiple acyl-CoA dehydrogenase deficiency
Jianying Xi et al.
JOURNAL OF INHERITED METABOLIC DISEASE (2014)
Wolman's Disease with Secondary Hemophagocytic Lymphohistiocytosis
F. Rabah et al.
PEDIATRIC HEMATOLOGY AND ONCOLOGY (2014)
Hemophagocytic syndrome in a 4-month-old infant with biotinidase deficiency
Fatih Kardas et al.
PEDIATRIC BLOOD & CANCER (2012)
Secondary Hemophagocytosis in 3 Patients With Organic Acidemia Involving Propionate Metabolism
M. Gokce et al.
PEDIATRIC HEMATOLOGY AND ONCOLOGY (2012)
Type II Gaucher disease manifesting as haemophagocytic lymphohistiocytosis
L. -R. Sharpe et al.
JOURNAL OF INHERITED METABOLIC DISEASE (2009)
Successful living-donor liver transplantation for Wilson's disease with Hemophagocytic syndrome
Satoshi Yokoyama et al.
TRANSPLANTATION (2007)
The myopathic form of coenzyme Q10 deficiency is caused by mutations in the electron-transferring-flavoprotein dehydrogenase (ETFDH) gene
Klaus Gempel et al.
BRAIN (2007)
First report of macrophage activation syndrome in hyperimmunoglobulinemia D with periodic fever syndrome
Donato Rigante et al.
ARTHRITIS AND RHEUMATISM (2007)
Lethal hemophagocytic lymphohistiocytosis in Hermansky-Pudlak syndrome type II
Anselm Enders et al.
BLOOD (2006)
Cobalamin C disease presenting with hemophagocytic lymphohistiocytosis
S Wu et al.
PEDIATRIC HEMATOLOGY AND ONCOLOGY (2005)
Pathomechanisms of neurodegeneration in glutaryl-CoA dehydrogenase deficiency
S Kolker et al.
ANNALS OF NEUROLOGY (2004)
Prospective screening for pediatric mitochondrial trifunctional protein defects in pregnancies complicated by liver disease
Z Yang et al.
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION (2002)