(Q36485435)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21748408%20AND%20SRC:MED&resulttype=core&format=json

7 February 2020

review article

1 reference

title

Combined methylmalonic acidemia and homocystinuria, cblC type. II. Complications, pathophysiology, and outcomes (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21748408%20AND%20SRC:MED&resulttype=core&format=json

7 February 2020

1 reference

methylmalonic acidemia

1 reference

1 reference

Nuria Carrillo-Carrasco

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21748408%20AND%20SRC:MED&resulttype=core&format=json

7 February 2020

author name string

Charles P Venditti

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21748408%20AND%20SRC:MED&resulttype=core&format=json

7 February 2020

publication date

12 July 2011

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21748408%20AND%20SRC:MED&resulttype=core&format=json

Journal of Inherited Metabolic Disease

7 February 2020

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21748408%20AND%20SRC:MED&resulttype=core&format=json

7 February 2020

volume

35

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21748408%20AND%20SRC:MED&resulttype=core&format=json

7 February 2020

issue

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21748408%20AND%20SRC:MED&resulttype=core&format=json

7 February 2020

page(s)

103-114

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21748408%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1007/s10545-011-9365-x

7 February 2020

exact match

0 references

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30 September 2017

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30 September 2017

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30 September 2017

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30 September 2017

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Genetic and cellular studies of oxidative stress in methylmalonic aciduria (MMA) cobalamin deficiency type C (cblC) with homocystinuria (MMACHC).

30 September 2017

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Profiling of oxidative stress in patients with inborn errors of metabolism

30 September 2017

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Fetal dilated cardiomyopathy: an unsuspected presentation of methylmalonic aciduria and hyperhomocystinuria, cblC type

30 September 2017

1 reference

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Cardiogenetics, neurogenetics, and pathogenetics of left ventricular hypertrabeculation/noncompaction

30 September 2017

1 reference

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Biochemical indicators of vitamin B12 and folate insufficiency and cognitive decline

30 September 2017

1 reference

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Murine models of hyperhomocysteinemia and their vascular phenotypes

30 September 2017

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Effect of folic acid and B vitamins on risk of cardiovascular events and total mortality among women at high risk for cardiovascular disease: a randomized trial

30 September 2017

1 reference

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Retinal dysfunction in combined methylmalonic aciduria and homocystinuria (Cblc) disease: a spectrum of disorders

30 September 2017

1 reference

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The adolescent and adult form of cobalamin C disease: clinical and molecular spectrum

30 September 2017

1 reference

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Hemolytic uremic syndrome (HUS) secondary to cobalamin C (cblC) disorder

30 September 2017

1 reference

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Role of redox reactions in the vascular phenotype of hyperhomocysteinemic animals

30 September 2017

1 reference

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The natural history of retinal degeneration in association with cobalamin C (cbl C) disease

30 September 2017

1 reference

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Cobalamin C disease presenting with hemophagocytic lymphohistiocytosis

30 September 2017

1 reference

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Disorders of intermediary metabolism: toxic leukoencephalopathies

30 September 2017

1 reference

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Late-onset thrombocytic microangiopathy caused by cblC disease: association with a factor H mutation

30 September 2017

1 reference

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Excitatory aminoacids and epileptic seizures in immature brain.

30 September 2017

1 reference

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Neuropsychiatric Disturbances in Presumed Late-Onset Cobalamin C Disease

30 September 2017

1 reference

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Cobalamin disorder Cbl-C presenting with late-onset thrombotic microangiopathy

30 September 2017

1 reference

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Cobalamin C disease presenting as hemolytic-uremic syndrome in the neonatal period

30 September 2017

1 reference

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Overexpression of cellular glutathione peroxidase rescues homocyst(e)ine-induced endothelial dysfunction

30 September 2017

1 reference

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Hyperhomocysteinemia enhances vascular inflammation and accelerates atherosclerosis in a murine model

30 September 2017

1 reference

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Early-onset combined methylmalonic aciduria and homocystinuria: neuroradiologic findings

30 September 2017

1 reference

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Endothelial dysfunction in a murine model of mild hyperhomocyst(e)inemia

30 September 2017

1 reference

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Homocysteine thiolactone: metabolic origin and protein homocysteinylation in humans

30 September 2017

1 reference

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Protein homocysteinylation: possible mechanism underlying pathological consequences of elevated homocysteine levels

30 September 2017

1 reference

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Tissue plasminogen activator binding to the annexin II tail domain. Direct modulation by homocysteine

30 September 2017

1 reference

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The association of protein-losing enteropathy with cobalamin C defect

30 September 2017

1 reference

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Hereditary defect of cobalamin metabolism (homocystinuria and methylmalonic aciduria) of juvenile onset

30 September 2017

1 reference

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Neonatal hemolytic-uremic syndrome, methylmalonic aciduria and homocystinuria caused by intracellular vitamin B 12 deficiency. Value of etiological diagnosis

30 September 2017

1 reference

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Congenital methylmalonic aciduria--homocystinuria with megaloblastic anemia: observations on response to hydroxocobalamin and on the effect of homocysteine and methionine on the deoxyuridine suppression test

30 September 2017

1 reference

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A derangement in B 12 metabolism leading to homocystinemia, cystathioninemia and methylmalonic aciduria

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3529128

Cor pulmonale as a complication of methylmalonic acidemia and homocystinuria (Cbl-C type).

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3529128

Cobalamin C defect associated with hemolytic-uremic syndrome

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3529128

A congenital anomaly of vitamin B12 metabolism: a study of three cases

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3529128

Congenital defect in intracellular cobalamin metabolism resulting in homocystinuria and methylmalonic aciduria. II. Biochemical investigations

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3529128

Homocysteine inhibits neoangiogenesis in mice through blockade of annexin A2-dependent fibrinolysis

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3529128

Resolution of cor pulmonale after medical management in a patient with cblC-type methylmalonic aciduria and homocystinuria: a case report

28 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3529128

Enhanced susceptibility to arterial thrombosis in a murine model of hyperhomocysteinemia.

28 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3529128

Elevated levels of homocysteine compromise blood-brain barrier integrity in mice

28 June 2018

1 reference

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Long-term outcome in treated combined methylmalonic acidemia and homocystinemia

28 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3529128

Progressive neurological deterioration and MRI changes in cblC methylmalonic acidaemia treated with hydroxocobalamin

28 June 2018

1 reference

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Anticonvulsant action of both NMDA and non-NMDA receptor antagonists against seizures induced by homocysteine in immature rats.

28 June 2018

1 reference

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Vascular pathology of homocysteinemia: implications for the pathogenesis of arteriosclerosis.

28 June 2018

1 reference

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An inborn error of vitamin B12 metabolism associated with cellular deficiency of coenzyme forms of the vitamin. Pathological and neurochemical findings in one case.

28 June 2018

1 reference

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Development of methyltransferase activities of human fetal tissues.

28 June 2018

1 reference

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Methylation deficiency causes vitamin B12-associated neuropathy in the pig.

28 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3529128

A cobalamin metabolic defect with homocystinuria, methylmalonic aciduria and macrocytic anemia.

28 June 2018

1 reference

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Distal motor axonopathy and central nervous system myelin vacuolation caused by cycloleucine, an inhibitor of methionine adenosyltransferase

28 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3529128

Disorders of creatine transport and metabolism.

28 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3529128

Early onset methylmalonic aciduria and homocystinuria cblC type with demyelinating neuropathy

21 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3529128

Effect of homocysteine-lowering B vitamin treatment on angiographic progression of coronary artery disease: a Western Norway B Vitamin Intervention Trial (WENBIT) substudy

21 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3529128

Cognitive and social profiles in two patients with cobalamin C disease.

21 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3529128

Hyperhomocysteinemia is associated with hypertriglyceridemia in mice with methylenetetrahydrofolate reductase deficiency.

21 September 2018

1 reference

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Creatine metabolism in combined methylmalonic aciduria and homocystinuria disease revisited.

21 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3529128

Late onset optic neuropathy in methylmalonic and propionic acidemia

21 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3529128

Ocular phenotype in patients with methylmalonic aciduria and homocystinuria, cobalamin C type

21 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3529128

Mild hyperhomocysteinemia is associated with increased TAFI levels and reduced plasma fibrinolytic potential

21 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3529128

Reduced brain choline in homocystinuria due to remethylation defects

21 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3529128

Retinopathy in inherited Transcobalamin II deficiency

21 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3529128

Late-onset combined homocystinuria and methylmalonic aciduria (cblC) and neuropsychiatric disturbance.

21 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3529128

Late-onset cobalamin-C disorder: a challenging diagnosis.

21 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3529128

Subacute combined degeneration of the spinal cord in cblC disorder despite treatment with B12.

21 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3529128

Modification of fibrinogen by homocysteine thiolactone increases resistance to fibrinolysis: a potential mechanism of the thrombotic tendency in hyperhomocysteinemia

21 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3529128

MRI and 1H-MRS findings in early-onset cobalamin C/D defect.

21 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3529128

Prenatal and postnatal treatment in cobalamin C defect

21 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3529128

Maculopathy and retinal degeneration in cobalamin C methylmalonic aciduria and homocystinuria

21 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3529128

Disturbed visual system function in methionine synthase deficiency

21 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3529128

Executive dysfunction in hyperhomocystinemia responds to homocysteine-lowering treatment

21 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3529128

Creatine metabolism in combined methylmalonic aciduria and homocystinuria

21 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3529128

Homocysteine down-regulates cellular glutathione peroxidase (GPx1) by decreasing translation

21 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3529128

Homocysteine induces oxidative stress by uncoupling of NO synthase activity through reduction of tetrahydrobiopterin.

21 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3529128

Perturbations in homocysteine-linked redox homeostasis in a murine model for hyperhomocysteinemia

21 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3529128

L-Homocysteine and L-homocystine stereospecifically induce endothelial nitric oxide synthase-dependent lipid peroxidation in endothelial cells

21 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3529128

Potential for misdiagnosis due to lack of metabolic derangement in combined methylmalonic aciduria/hyperhomocysteinemia (cblC) in the neonate

21 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3529128

High exogenous homocysteine modifies eye development in early chick embryos

21 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3529128

Increased superoxide production in coronary arteries in hyperhomocysteinemia: role of tumor necrosis factor-alpha, NAD(P)H oxidase, and inducible nitric oxide synthase

21 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3529128

Cobalamin C deficiency complicated by an atypical glomerulopathy

21 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3529128

Homocysteine is a protein amino acid in humans. Implications for homocysteine-linked disease

21 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3529128

Early-onset cobalamin C/D deficiency: epilepsy and electroencephalographic features.

21 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3529128

Adult-onset combined methylmalonic aciduria and homocystinuria (cblC).

21 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3529128

Neurological and neuropathologic heterogeneity in two brothers with cobalamin C deficiency.

21 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3529128

Demyelination and inborn errors of the single carbon transfer pathway.

21 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3529128

Homocysteic and homocysteine sulphinic acid exhibit excitotoxicity in organotypic cultures from rat brain.

21 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3529128

Methylmalonic acidemia, cobalamin C type, presenting with cutaneous manifestations

21 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3529128

Clinical heterogeneity and prognosis in combined methylmalonic aciduria and homocystinuria (cblC).

21 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3529128

Protective effects of methylcobalamin, a vitamin B12 analog, against glutamate-induced neurotoxicity in retinal cell culture.

21 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3529128

Seizures induced by homocysteine in rats during ontogenesis.

21 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3529128

Retinal degeneration in vitamin B12 disorder associated with methylmalonic aciduria and sulfur amino acid abnormalities

21 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3529128

Pathogenesis of subacute combined degeneration: a result of methyl group deficiency

21 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3529128

Transfer of Cyst(e)ine and Methionine across the Human Placenta

21 September 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS10545-011-9365-X

Treatment responsive executive and behavioral dysfunction associated with Vitamin B12 deficiency

21 January 2018

1 reference

12 December 2020

Optic atrophy in association with cobalamin C (cblC) disease

1 reference

12 December 2020

Optic neuropathy in methylmalonic acidemia: the role of neuroprotection

1 reference

12 December 2020

Clinical heterogeneity in cobalamin C variant of combined homocystinuria and methylmalonic aciduria

1 reference

12 December 2020

Expanded newborn screening

1 reference

12 December 2020

Mutations in methylenetetrahydrofolate reductase or cystathionine beta-synthase gene, or a high-methionine diet, increase homocysteine thiolactone levels in humans and mice

1 reference

12 December 2020

Congenital defect in intracellular cobalamin metabolism resulting in homocysteinuria and methylmalonic aciduria. I. Case report and histopathology

1 reference

12 December 2020

Clinical trials: curing a critical deficiency in metabolic medicine

1 reference

12 December 2020

Evidence based medicine in inborn errors of metabolism: is there any and how to find it

1 reference

12 December 2020

Epileptiform ocular movements with methylmalonic aciduria and homocystinuria

1 reference

12 December 2020

Cobalamin C mutation (methylmalonic aciduria and homocystinuria) in adolescence. A treatable cause of dementia and myelopathy

1 reference

12 December 2020

Reversible dementia in an adolescent with cblC disease: clinical heterogeneity within the same family

1 reference

12 December 2020

Homocyst(e)ine decreases bioavailable nitric oxide by a mechanism involving glutathione peroxidase

1 reference

12 December 2020

Homocysteine and thrombosis: from basic science to clinical evidence

1 reference

12 December 2020

Ocular histopathologic characteristics of cobalamin C type vitamin B12 defect with methylmalonic aciduria and homocystinuria

1 reference

12 December 2020

Metabolism of homocysteine thiolactone in human cell cultures. Possible mechanism for pathological consequences of elevated homocysteine levels

1 reference

12 December 2020

Homocysteine-induced endothelial cell injury in vitro: a model for the study of vascular injury

1 reference

12 December 2020

Homocysteine and vascular disease

1 reference

12 December 2020

10.1007/S10545-011-9365-X

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21748408%20AND%20SRC:MED&resulttype=core&format=json

7 February 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21748408%20AND%20SRC:MED&resulttype=core&format=json

7 February 2020

1 reference