(Q31072456)

English

Glucosylceramide transfer from lysosomes--the missing link in molecular pathology of glucosylceramidase deficiency: a hypothesis based on existing data

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scholarly article

1 reference

Europe PubMed Central

28 June 2017

Glucosylceramide transfer from lysosomes--the missing link in molecular pathology of glucosylceramidase deficiency: a hypothesis based on existing data (English)

1 reference

Europe PubMed Central

28 June 2017

0 references

author name string

Elleder M

1

1 reference

Europe PubMed Central

28 June 2017

publication date

2 November 2006

1 reference

Europe PubMed Central

28 June 2017

Journal of Inherited Metabolic Disease

1 reference

Europe PubMed Central

28 June 2017

29

1 reference

Europe PubMed Central

28 June 2017

6

1 reference

Europe PubMed Central

28 June 2017

707-715

1 reference

Europe PubMed Central

28 June 2017

https://scigraph.springernature.com/pub.10.1007/s10545-006-0411-z

0 references

Enzymic effects of β-glucosidase destruction in mice changes in glucuronidase levels

1 reference

https://api.crossref.org/works/10.1007%2FS10545-006-0411-Z

21 January 2018

The occurrence of psychosine and other glycolipids in spleen and liver from the three major types of Gaucher's disease

1 reference

https://api.crossref.org/works/10.1007%2FS10545-006-0411-Z

21 January 2018

The NPC1 protein: structure implies function.

1 reference

https://api.crossref.org/works/10.1007%2FS10545-006-0411-Z

21 January 2018

Demonstration of the existence of a second, non-lysosomal glucocerebrosidase that is not deficient in Gaucher disease

1 reference

https://api.crossref.org/works/10.1007%2FS10545-006-0411-Z

21 January 2018

Skeletal aspects of Gaucher disease: a review

1 reference

https://api.crossref.org/works/10.1007%2FS10545-006-0411-Z

21 January 2018

Viable mouse models of acid beta-glucosidase deficiency: the defect in Gaucher disease

1 reference

https://api.crossref.org/works/10.1007%2FS10545-006-0411-Z

21 January 2018

Gaucher disease with parkinsonian manifestations: does glucocerebrosidase deficiency contribute to a vulnerability to parkinsonism?

1 reference

https://pubmed.ncbi.nlm.nih.gov/17080304

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Gaucher's disease: clinical features and natural history

1 reference

https://pubmed.ncbi.nlm.nih.gov/17080304

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Gaucher's disease type I. Report of a case with prominent deposition of ceroid in splenic endothelial cells and intestinal smooth muscle fibers

1 reference

https://pubmed.ncbi.nlm.nih.gov/17080304

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Unusual echocardiographic pattern in Gaucher's disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/17080304

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Glucosylceramide synthesis and synthase expression protect against ceramide-induced stress.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17080304

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Bone ultrasonometry, bone density, and turnover markers in type 1 Gaucher disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/17080304

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Glucosylceramides stimulate murine epidermal hyperproliferation.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17080304

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Severe valvular and aortic arch calcification in a patient with Gaucher's disease homozygous for the D409H mutation

1 reference

https://pubmed.ncbi.nlm.nih.gov/17080304

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Neonatal Gaucher disease presenting as persistent thrombocytopenia

1 reference

https://pubmed.ncbi.nlm.nih.gov/17080304

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

In vitro accumulation of glucocerebroside in neuroblastoma cells: a model for study of Gaucher disease pathobiology

1 reference

https://pubmed.ncbi.nlm.nih.gov/17080304

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Congenital ichthyosis with restrictive dermopathy and Gaucher disease: a new syndrome with associated prenatal diagnostic and pathology findings

1 reference

https://pubmed.ncbi.nlm.nih.gov/17080304

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Gaucher's disease with myocardial involvement in pregnancy

1 reference

https://pubmed.ncbi.nlm.nih.gov/17080304

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A patient with type 2 Gaucher's disease with respiratory disease.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17080304

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Fundus abnormalities in a patient with type I Gaucher's disease with 12-year follow-up

1 reference

https://pubmed.ncbi.nlm.nih.gov/17080304

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Niemann-Pick disease type C.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17080304

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A chimeric mouse model of Gaucher disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/17080304

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Type 3 GM1 gangliosidosis: characteristic MRI findings correlated with dystonia

1 reference

https://pubmed.ncbi.nlm.nih.gov/17080304

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Histochemical and ultrastructural study of Gaucher cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/17080304

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Unusual cardiac, renal and pulmonary involvement in Gaucher's disease. Intersitial glucocerebroside accumulation, pulmonary hypertension and fatal bone marrow embolization

1 reference

https://pubmed.ncbi.nlm.nih.gov/17080304

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A new variant neuropathic type of Gaucher's disease characterized by hydrocephalus, corneal opacities, deformed toes, and fibrous thickening of spleen and liver capsules

1 reference

https://pubmed.ncbi.nlm.nih.gov/17080304

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Infantile neurological Gaucher's disease in three siblings. An ultrastructural study.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17080304

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Skeletal complications of Gaucher disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/17080304

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Binding, internalization, and degradation of mannose-terminated glucocerebrosidase by macrophages

1 reference

https://pubmed.ncbi.nlm.nih.gov/17080304

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Marked elevation of plasma chitotriosidase activity. A novel hallmark of Gaucher disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/17080304

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Sphingosylphosphorylcholine in Niemann-Pick disease brain: accumulation in type A but not in type B.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17080304

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Gaucher disease: complexity in a "simple" disorder

1 reference

https://pubmed.ncbi.nlm.nih.gov/17080304

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Light microscopic and ultrastructural study on CNS lesions in infantile Gaucher's disease.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17080304

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Perinatal-lethal Gaucher disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/17080304

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Vascular involvement in type 3 neuronopathic Gaucher's disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/17080304

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Toxicity of glucosylsphingosine (glucopsychosine) to cultured neuronal cells: a model system for assessing neuronal damage in Gaucher disease type 2 and 3.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17080304

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A rat brain cytosol protein which accelerates the translocation of galactosylceramide, lactosylceramide and glucosylceramide between membranes.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17080304

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prosaposin deficiency -- a rarely diagnosed, rapidly progressing, neonatal neurovisceral lipid storage disease. Report of a further patient.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17080304

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Lysosomal non-lipid component of Gaucher’s cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/17080304

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Synthesis of cerebroside by brain from uridine diphosphate galactose and ceramide containing hydroxy fatty acid

1 reference

https://pubmed.ncbi.nlm.nih.gov/17080304

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Consequences of beta-glucocerebrosidase deficiency in epidermis. Ultrastructure and permeability barrier alterations in Gaucher disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/17080304

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clinical evaluation of chemokine and enzymatic biomarkers of Gaucher disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/17080304

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Gaucher disease in mice induced by conduritol-B-epoxide: morphologic features

1 reference

https://pubmed.ncbi.nlm.nih.gov/17080304

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The fate of glucosylceramide (glucocerebroside) in genetically impaired (lysosomal beta-glucosidase deficient) Gaucher disease diploid human fibroblasts

1 reference

https://pubmed.ncbi.nlm.nih.gov/17080304

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Biosynthesis of galactosylsphingosine (psychosine) in the twitcher mouse.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17080304

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Enhanced calcium release in the acute neuronopathic form of Gaucher disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/17080304

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Stimulation of liver growth and DNA synthesis by glucosylceramide

1 reference

https://pubmed.ncbi.nlm.nih.gov/17080304

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Macular changes in type I Gaucher's disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/17080304

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A biochemical and ultrastructural evaluation of the type 2 Gaucher mouse.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17080304

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Modulation of renal epithelial cell growth by glucosylceramide. Association with protein kinase C, sphingosine, and diacylglycerol

1 reference

https://pubmed.ncbi.nlm.nih.gov/17080304

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Retinal involvement in Gaucher's disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/17080304

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Dexamethasone-Mediated Up-Regulation of the Mannose Receptor Improves the Delivery of Recombinant Glucocerebrosidase to Gaucher Macrophages

1 reference

https://pubmed.ncbi.nlm.nih.gov/17080304

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The fate and function of glycosphingolipid glucosylceramide

1 reference

https://pubmed.ncbi.nlm.nih.gov/17080304

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Gaucher disease: understanding the molecular pathogenesis of sphingolipidoses

1 reference

https://pubmed.ncbi.nlm.nih.gov/17080304

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Glucosylceramide uptake protein from spleen cytosol

1 reference

https://pubmed.ncbi.nlm.nih.gov/17080304

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Sphingolipid activator protein deficiency in a 16-week-old atypical Gaucher disease patient and his fetal sibling: biochemical signs of combined sphingolipidoses

1 reference

https://pubmed.ncbi.nlm.nih.gov/17080304

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Enzyme replacement therapy for Gaucher disease: skeletal responses to macrophage-targeted glucocerebrosidase

1 reference

https://pubmed.ncbi.nlm.nih.gov/17080304

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Systemic inflammation in glucocerebrosidase-deficient mice with minimal glucosylceramide storage

1 reference

https://pubmed.ncbi.nlm.nih.gov/17080304

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Infantile Gaucher's disease: a case with neuronal storage

1 reference

https://pubmed.ncbi.nlm.nih.gov/17080304

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Pulmonary hypertension and Gaucher's disease: logical association or mere coincidence?

1 reference

https://pubmed.ncbi.nlm.nih.gov/17080304

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Biochemical studies in a patient with subacute neuropathic Gaucher disease without visceral glucosylceramide storage.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17080304

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The organizing potential of sphingolipids in intracellular membrane transport

1 reference

https://pubmed.ncbi.nlm.nih.gov/17080304

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Elevation of intracellular glucosylceramide levels results in an increase in endoplasmic reticulum density and in functional calcium stores in cultured neurons.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17080304

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Effectiveness of enzyme replacement therapy in 1028 patients with type 1 Gaucher disease after 2 to 5 years of treatment: a report from the Gaucher Registry

1 reference

https://pubmed.ncbi.nlm.nih.gov/17080304

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Topography of glycosyltransferases involved in the initial glycosylations of gangliosides

1 reference

https://pubmed.ncbi.nlm.nih.gov/17080304

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A novel mutation in the coding region of the prosaposin gene leads to a complete deficiency of prosaposin and saposins, and is associated with a complex sphingolipidosis dominated by lactosylceramide accumulation

1 reference

https://pubmed.ncbi.nlm.nih.gov/17080304

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Fine structure of central nervous system in early infantile Gaucher's disease.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17080304

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Characterization of the Cytoplasmic Inclusion Bodies of the Spleens from Patients with Adult Form Gaucher′s Disease1

1 reference

https://pubmed.ncbi.nlm.nih.gov/17080304

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Niemann-Pick disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/17080304

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Reactions of vessel walls and brain parenchyma to the accumulation of Gaucher cells in the Norrbottnian type (type III) of Gaucher disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/17080304

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Metabolism of glucosyl [13H]ceramide by human skin fibroblasts from normal and glucosylceramidotic subjects

1 reference

https://pubmed.ncbi.nlm.nih.gov/17080304

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Integration of glycosphingolipid metabolism and cell-fate decisions in cancer and stem cells: review and hypothesis

1 reference

https://pubmed.ncbi.nlm.nih.gov/17080304

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Incidence of malignancies among patients with type I Gaucher disease from a single referral clinic.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17080304

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cardiac involvement by Gaucher's disease documented by right ventricular endomyocardial biopsy

1 reference

https://pubmed.ncbi.nlm.nih.gov/17080304

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Pathologic gene expression in Gaucher disease: up-regulation of cysteine proteinases including osteoclastic cathepsin K.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17080304

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

ER retention and degradation as the molecular basis underlying Gaucher disease heterogeneity

1 reference

https://pubmed.ncbi.nlm.nih.gov/17080304

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Collodion babies with Gaucher's disease--a further case

1 reference

https://pubmed.ncbi.nlm.nih.gov/17080304

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Relationships between serum markers of monocyte/macrophage activation in type 1 Gaucher's disease.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17080304

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Enzyme replacement therapy reduces Gaucher cell burden but may accelerate osteopenia in patients with type I disease - a histological study

1 reference

https://pubmed.ncbi.nlm.nih.gov/17080304

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Impaired trafficking of mutants of lysosomal glucocerebrosidase in Gaucher's disease.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17080304

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Gaucher disease: Perspectives on a prototype lysosomal disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/17080304

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Neuropathology provides clues to the pathophysiology of Gaucher disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/17080304

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Generation of specific deoxynojirimycin-type inhibitors of the non-lysosomal glucosylceramidase

1 reference

https://pubmed.ncbi.nlm.nih.gov/17080304

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Variant Gaucher disease characterized by dysmorphic features, absence of cardiovascular involvement, laryngospasm, and compound heterozygosity for a novel mutation (D409H/C16S).

1 reference

https://pubmed.ncbi.nlm.nih.gov/17080304

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Gaucher's disease and chronic lymphocytic leukemia. Possible pathogenetic link between Gaucher's disease and B-cell proliferations?

1 reference

https://pubmed.ncbi.nlm.nih.gov/17080304

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The neuropathology of infantile Gaucher's disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/17080304

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Glycolipid transfer protein from bovine brain.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17080304

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Pulmonary hypertension in type 1 Gaucher's disease: genetic and epigenetic determinants of phenotype and response to therapy

1 reference

https://pubmed.ncbi.nlm.nih.gov/17080304

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The pathogenesis of glycosphingolipid storage disorders

1 reference

https://pubmed.ncbi.nlm.nih.gov/17080304

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Animal model of Gaucher's disease from targeted disruption of the mouse glucocerebrosidase gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/17080304

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

GM1-ganglioside-mediated activation of the unfolded protein response causes neuronal death in a neurodegenerative gangliosidosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/17080304

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Lyso-glycosphingolipids mobilize calcium from brain microsomes via multiple mechanisms

1 reference

https://pubmed.ncbi.nlm.nih.gov/17080304

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Phosphatidylcholine synthesis is elevated in neuronal models of Gaucher disease due to direct activation of CTP:phosphocholine cytidylyltransferase by glucosylceramide

1 reference

https://pubmed.ncbi.nlm.nih.gov/17080304

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Gaucher disease: pathological mechanisms and modern management

1 reference

https://pubmed.ncbi.nlm.nih.gov/17080304

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Abnormal expression of the novel epidermal enzyme, glucosylceramide deacylase, and the accumulation of its enzymatic reaction product, glucosylsphingosine, in the skin of patients with atopic dermatitis.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17080304

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Substrate reduction therapy for lysosomal storage diseases

1 reference

https://pubmed.ncbi.nlm.nih.gov/17080304

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Glucosylsphingosine accumulation in mice and patients with type 2 Gaucher disease begins early in gestation

1 reference

https://pubmed.ncbi.nlm.nih.gov/17080304

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The synthetic pathway for glucosylsphingosine in cultured fibroblasts

1 reference

https://pubmed.ncbi.nlm.nih.gov/17080304

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An ultrastructural and experimental study on the development of tubular structures in the lysosomes of Gaucher cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/17080304

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Gaucher disease in the neonate: a distinct Gaucher phenotype is analogous to a mouse model created by targeted disruption of the glucocerebrosidase gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/17080304

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cardiovascular fibrosis, hydrocephalus, ophthalmoplegia, and visceral involvement in an American child with Gaucher disease.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17080304

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Glucosylsphingosine accumulation in tissues from patients with Gaucher disease: correlation with phenotype and genotype

1 reference

https://pubmed.ncbi.nlm.nih.gov/17080304

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Late-infantile Gaucher disease in a child with myoclonus and bulbar signs: neuropathological and neurochemical findings

1 reference

https://pubmed.ncbi.nlm.nih.gov/17080304

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Gaucher cells demonstrate a distinct macrophage phenotype and resemble alternatively activated macrophages

1 reference

https://pubmed.ncbi.nlm.nih.gov/17080304

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Perinatal lethal Gaucher disease: a distinct phenotype along the neuronopathic continuum

1 reference

https://pubmed.ncbi.nlm.nih.gov/17080304

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S10545-006-0411-Z

1 reference

Europe PubMed Central

28 June 2017

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1 reference

Europe PubMed Central

28 June 2017

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0 references

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