Acute liver failure after valproate exposure in patients with POLG1 mutations and the prognosis after liver transplantation. (Q54334767)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25065347%20AND%20SRC:MED&resulttype=core&format=json

10 March 2020

title

Acute liver failure after valproate exposure in patients with POLG1 mutations and the prognosis after liver transplantation (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25065347%20AND%20SRC:MED&resulttype=core&format=json

10 March 2020

main subject

liver transplantation

1 reference

1 reference

9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25065347%20AND%20SRC:MED&resulttype=core&format=json

10 March 2020

8

Matias Röyttä

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25065347%20AND%20SRC:MED&resulttype=core&format=json

10 March 2020

5

Johanna Arola

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25065347%20AND%20SRC:MED&resulttype=core&format=json

10 March 2020

author name string

Johanna Hynynen

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25065347%20AND%20SRC:MED&resulttype=core&format=json

10 March 2020

Tuomas Komulainen

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25065347%20AND%20SRC:MED&resulttype=core&format=json

10 March 2020

Eija Tukiainen

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25065347%20AND%20SRC:MED&resulttype=core&format=json

10 March 2020

Arno Nordin

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25065347%20AND%20SRC:MED&resulttype=core&format=json

10 March 2020

Reetta Kälviäinen

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25065347%20AND%20SRC:MED&resulttype=core&format=json

10 March 2020

Leena Jutila

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25065347%20AND%20SRC:MED&resulttype=core&format=json

10 March 2020

Kari Majamaa

10

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25065347%20AND%20SRC:MED&resulttype=core&format=json

10 March 2020

Heikki Mäkisalo

11

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25065347%20AND%20SRC:MED&resulttype=core&format=json

10 March 2020

Johanna Uusimaa

12

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25065347%20AND%20SRC:MED&resulttype=core&format=json

10 March 2020

publication date

3 October 2014

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25065347%20AND%20SRC:MED&resulttype=core&format=json

10 March 2020

published in

Liver Transplantation

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25065347%20AND%20SRC:MED&resulttype=core&format=json

10 March 2020

volume

20

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25065347%20AND%20SRC:MED&resulttype=core&format=json

10 March 2020

issue

11

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25065347%20AND%20SRC:MED&resulttype=core&format=json

10 March 2020

page(s)

1402-1412

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25065347%20AND%20SRC:MED&resulttype=core&format=json

DNA polymerase gamma, the mitochondrial replicase

10 March 2020

cites work

1 reference

DNA polymerase gamma and mitochondrial disease: understanding the consequence of POLG mutations.

21 January 2018

1 reference

Mitochondrial DNA polymerase gamma deficiency and mtDNA depletion in a child with Alpers' syndrome.

21 January 2018

1 reference

Molecular diagnosis of Alpers syndrome.

21 January 2018

1 reference

Alpers syndrome: progressive neuronal degeneration of children with liver disease

21 January 2018

1 reference

Mitochondrial hepatopathies: advances in genetics and pathogenesis

21 January 2018

1 reference

Homozygous W748S mutation in the POLG1 gene in patients with juvenile-onset Alpers syndrome and status epilepticus

21 January 2018

1 reference

Mitochondrial DNA depletion syndromes: review and updates of genetic basis, manifestations, and therapeutic options

21 January 2018

1 reference

Polymerase gamma 1 mutations: clinical correlations

21 January 2018

1 reference

Early childhood hepatocerebral degeneration misdiagnosed as valproate hepatotoxicity

21 January 2018

1 reference

Inappropriate liver transplantation in a child with Alpers-Huttenlocher syndrome misdiagnosed as valproate-induced acute liver failure

21 January 2018

1 reference

Fatal deterioration of neurological disease after orthotopic liver transplantation for valproic acid-induced liver damage.

21 January 2018

1 reference

Reversible valproate hepatotoxicity due to mutations in mitochondrial DNA polymerase γ (POLG1)

21 January 2018

1 reference

POLG DNA testing as an emerging standard of care before instituting valproic acid therapy for pediatric seizure disorders

21 January 2018

1 reference

Polymerase γ gene POLG determines the risk of sodium valproate-induced liver toxicity

21 January 2018

1 reference

The spectrum of clinical disease caused by the A467T and W748S POLG mutations: a study of 26 cases

21 January 2018

1 reference

POLG1 mutations cause a syndromic epilepsy with occipital lobe predilection

21 January 2018

1 reference

Prospective study of POLG mutations presenting in children with intractable epilepsy: prevalence and clinical features.

21 January 2018

1 reference

Clinical and molecular features of mitochondrial DNA depletion syndromes.

21 January 2018

1 reference

Liver transplantation in mitochondrial respiratory chain disorders

21 January 2018

1 reference

DNA extraction procedures meaningfully influence qPCR-based mtDNA copy number determination

21 January 2018

1 reference

Detection and quantification of mitochondrial DNA deletions in individual cells by real-time PCR.

21 January 2018

1 reference

A new mathematical model for relative quantification in real-time RT-PCR

21 January 2018

1 reference

Diagnosis of mitochondrial DNA depletion syndromes

21 January 2018

1 reference

Standardization of nomenclature and causality assessment in drug-induced liver injury: summary of a clinical research workshop

21 January 2018

1 reference

Mitochondrial DNA polymerase W748S mutation: a common cause of autosomal recessive ataxia with ancient European origin

21 January 2018

1 reference

Modulation of the W748S mutation in DNA polymerase gamma by the E1143G polymorphismin mitochondrial disorders

21 January 2018

1 reference

Autosomal recessive mitochondrial ataxic syndrome due to mitochondrial polymerase gamma mutations

21 January 2018

1 reference

Rapidly progressive neurological deterioration in a child with Alpers syndrome exhibiting a previously unremarkable brain MRI.

21 January 2018

1 reference

Molecular and clinical genetics of mitochondrial diseases due to POLG mutations

21 January 2018

1 reference

POLG1 manifestations in childhood

21 January 2018

1 reference

Functional defects due to spacer-region mutations of human mitochondrial DNA polymerase in a family with an ataxia-myopathy syndrome

21 January 2018

1 reference

Analysis of mutant DNA polymerase gamma in patients with mitochondrial DNA depletion.

21 January 2018

1 reference

Infantile hepatocerebral syndromes associated with mutations in the mitochondrial DNA polymerase-gammaA.

21 January 2018

1 reference

Phenotypic spectrum associated with mutations of the mitochondrial polymerase gamma gene

21 January 2018

1 reference

A novel POLG gene mutation in 4 children with Alpers-like hepatocerebral syndromes

21 January 2018

1 reference

Reduced mitochondrial DNA content and heterozygous nuclear gene mutations in patients with acute liver failure.

21 January 2018

1 reference

Carnitine in the treatment of valproic acid-induced toxicity

21 January 2018

1 reference

Effect of L-carnitine treatment for valproate-induced hepatotoxicity

21 January 2018

1 reference

l-Carnitine Supplementation in Childhood Epilepsy: Current Perspectives

21 January 2018

1 reference

Status epilepticus in children with Alpers' disease caused by POLG1 mutations: EEG and MRI features

21 January 2018

1 reference