(Q41927652)

14 October 2017

title

Acute pancreatitis in an infant with lactic acidosis and a mutation at nucleotide 3243 in the mitochondrial DNA tRNALeu(UUR) gene (English)

1 reference

14 October 2017

0 references

1 reference

P S Kishnani

1

1 reference

14 October 2017

J L Van Hove

2

1 reference

14 October 2017

J S Shoffner

3

1 reference

14 October 2017

A Kaufman

4

1 reference

14 October 2017

E H Bossen

5

1 reference

14 October 2017

S G Kahler

6

1 reference

14 October 2017

publication date

1 October 1996

1 reference

European Journal of Pediatrics

14 October 2017

published in

1 reference

14 October 2017

volume

155

1 reference

14 October 2017

issue

10

1 reference

14 October 2017

page(s)

898-903

1 reference

Update on laboratory diagnosis and prognosis of acute pancreatitis

14 October 2017

cites work

1 reference

12 December 2020

Superoxide anions and hyperoxia inactivate endothelium-derived relaxing factor

1 reference

12 December 2020

Clinicopathologic studies in childhood pancreatitis

1 reference

12 December 2020

Procedure for the histochemical demonstration of actomyosin ATPase

1 reference

12 December 2020

Maternally inherited diabetes and deafness is a distinct subtype of diabetes and associates with a single point mutation in the mitochondrial tRNA(Leu(UUR)) gene

1 reference

12 December 2020

Fatal infantile cytochrome c oxidase deficiency: decrease of immunologically detectable enzyme in muscle

1 reference

12 December 2020

A histochemical method for the demonstration of diphosphopyridine nucleotide diaphorase

1 reference

12 December 2020

Mitochondrial diabetes mellitus: prevalence and clinical characterization of diabetes due to mitochondrial tRNA(Leu(UUR)) gene mutation in Japanese patients

1 reference

12 December 2020

A mutation in the tRNA(Leu)(UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathies

1 reference

12 December 2020

Pearson's marrow-pancreas syndrome. A multisystem mitochondrial disorder in infancy

1 reference

12 December 2020

Chronic pancreatitis in a child with glycogen storage disease type 1

1 reference

12 December 2020

MELAS of infantile onset: mitochondrial angiopathy or cytopathy?

1 reference

12 December 2020

Lipase isoforms and amylase isoenzymes: assays and application in the diagnosis of acute pancreatitis.

1 reference

12 December 2020

The high prevalence of the diabetic patients with a mutation in the mitochondrial gene in Japan

1 reference

12 December 2020

Mitochondrial encephalomyopathy, lactic acidosis, stroke-like episodes (MELAS): clinical, radiological, pathological, and genetic observations

1 reference

12 December 2020

Chronic pancreatitis in muscular cytochrome c oxidase deficiency

1 reference

12 December 2020

Acute pancreatitis and normoamylasemia. Not an uncommon combination

1 reference

12 December 2020

Familial recurrence of atypical symptoms in an extended pedigree with the syndrome of mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes (MELAS)

1 reference

12 December 2020

Mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes: A distinctive clinical syndrome

1 reference

12 December 2020

Drug-induced pancreatitis

1 reference

12 December 2020

Widespread multitissue deletions of the mitochondrial genome in the Pearson marrow-pancreas syndrome

1 reference

12 December 2020

Normal amylase levels in the presentation of acute pancreatitis

1 reference

12 December 2020

Combined diagnostic value of biochemical markers in acute pancreatitis

1 reference

12 December 2020

MELAS: clinical features, biochemistry, and molecular genetics

1 reference

12 December 2020

Genotype to phenotype correlations in mitochondrial encephalomyopathies associated with the A3243G mutation of mitochondrial DNA

1 reference

12 December 2020

Pancreatic disorders in infancy and childhood: experience with 92 cases.

1 reference

12 December 2020

The clinical features of mitochondrial myopathy

1 reference

12 December 2020

Subacute necrotizing encephalopathy: oxidative phosphorylation defects and the ATPase 6 point mutation

1 reference

12 December 2020

Deletion of mitochondrial DNA in a case of early-onset diabetes mellitus, optic atrophy, and deafness (Wolfram syndrome, MIM 222300).

1 reference

12 December 2020

A child with acute pancreatitis and recurrent hypoglycemia due to 3-hydroxy-3-methylglutaryl-CoA lyase deficiency

1 reference

12 December 2020

Mitochondrial gene defects in patients with NIDDM

1 reference

12 December 2020

Acute pancreatitis in childhood

1 reference

12 December 2020

A subtype of diabetes mellitus associated with a mutation of mitochondrial DNA.

1 reference

12 December 2020

Carnitine palmitoyltransferase II deficiency: a new cause of recurrent pancreatitis

1 reference

12 December 2020

RAPID EXAMINATION OF MUSCLE TISSUE. AN IMPROVED TRICHROME METHOD FOR FRESH-FROZEN BIOPSY SECTIONS

1 reference

12 December 2020

Pancreatitis in patients with organic acidemias

1 reference

12 December 2020

Identifiers

DOI

10.1007/S004310050511

1 reference

14 October 2017

1 reference