The occurrence of hepatoma in the chronic form of hereditary tyrosinemia (Q34578074)

3 August 2017

title

The occurrence of hepatoma in the chronic form of hereditary tyrosinemia (English)

1 reference

3 August 2017

main subject

hepatocellular carcinoma

1 reference

A. G. Weinberg

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A173827

21 May 2022

C. E. Mize

series ordinal

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A173827

21 May 2022

H. G. Worthen

series ordinal

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A173827

21 May 2022

language of work or name

English

0 references

1 March 1976

1 reference

full work available at URL

3 August 2017

https://api.elsevier.com/content/article/PII:S0022347676802594?httpAccept=text/xml

1 reference

https://api.crossref.org/works/10.1016/S0022-3476(76)80259-4

https://api.elsevier.com/content/article/PII:S0022347676802594?httpAccept=text/plain

21 May 2022

1 reference

https://api.crossref.org/works/10.1016/S0022-3476(76)80259-4

The Journal of Pediatrics

21 May 2022

published in

1 reference

3 August 2017

1 reference

3 August 2017

1 reference

3 August 2017

page(s)

434-438

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STUDIES ON TYROSINOSIS: 2, ACTIVITY OF THE TRANSAMINASE, PARAHYDROXY-PHENYL-PYRUVATE OXIDASE, AND HOMOGENTISIC-ACID OXIDASE

3 August 2017

cites work

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7 January 2021

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Long-term dietary treatment of tyrosinosis

7 January 2021

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Tyrosinemia with plantar and palmar keratosis and keratitis

7 January 2021

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Biochemical observations on so-called hereditary tyrosinemia

7 January 2021

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Urinary phenolic acids in tyrosinemia. identification and quantitation by gas chromatographymass spectrometry

7 January 2021

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Hereditary tyrosinemia and abnormal pyrrolemetabolism

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Diagnosis and treatment of tyrosinosis

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Malignant liver tumors in children

7 January 2021

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STUDIES ON TYROSINOSIS: 1, EFFECT OF LOW-TYROSINE AND LOW-PHENYLALANINE DIET

7 January 2021

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Tyrosinosis. A study of 6 cases

7 January 2021

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FAMILIAL CIRRHOSIS OF THE LIVER, RENAL TUBULAR DEFECTS WITH RICKETS AND IMPAIRED TYROSINE METABOLISM

7 January 2021

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Dietary treatment in tyrosinemia (tyrosinosis). With a note on the possible recognition of the carrier state

7 January 2021

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Excretion of δ-aminolevulinic acid in hereditary tyrosinemia

7 January 2021

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Enzymatic studies in a case of hereditary tyrosinemia with hepatoma

7 January 2021

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A case of congenital cirrhosis of the liver with renal tubular defects akin to those in the Fanconi syndrome

7 January 2021

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Hepatoblastoma and hepatocarcinoma in infancy and childhood. Report of 47 cases

7 January 2021

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Primary carcinoma of the liver after giant-cell hepatitis of infancy; report of a case

7 January 2021

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Hepatic cirrhosis: a clinico-pathological review of 520 cases

7 January 2021

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-fetoprotein in indian childhood cirrhosis

7 January 2021

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7 January 2021

Jikeikai medical journal

An atypical case of tyrosinosis. III. The outcome of the patient: pathological and biochemical observations on the organ tissues (English)

Sakai

1959

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Zeitschrift fur Kinderheilkunde

21 May 2022

113

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Tyrosinose. Primäre and sekundäre biochemische Veränderungen (English)

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1972

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21 May 2022

Jikeikai medical journal

An atypical case of tyrosinosis. I. Clinical and laboratory findings (English)

Sakai

1957

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21 May 2022

Jikeikai medical journal

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A propos d'un cas de tyrosynurie avec cirrhose congenitale et tubulopathie (English)

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1965

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21 May 2022

935

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21 May 2022

171

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1972

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Pathology and Biology

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Tyrosinémie héréditaire et alpha-1-foetoprotéine. I. Intérét clinique de l'alpha-foeto-protéine dans la tyrosinémie héréditaire (English)

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1973

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Tyrosinosis: a new variant

21 May 2022

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Clinical and biochemical study of three patients with tyrosyluria

22 December 2022

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Studies on the mechanism of the Fanconi syndrome

22 December 2022

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Hepatocarcinoma associated with biliary cirrhosis. A case due to congenital bile duct atresia

22 December 2022

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22 December 2022

Identifiers

1 reference

3 August 2017

1 reference