(Q50776530)

19 March 2018

title

Long-term outcome and intervention of urea cycle disorders in Japan. (English)

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19 March 2018

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11

Reiko Horikawa

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19 March 2018

author name string

Jun Kido

1

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19 March 2018

Kimitoshi Nakamura

2

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19 March 2018

Hiroshi Mitsubuchi

3

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19 March 2018

Toshihiro Ohura

4

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19 March 2018

Masaki Takayanagi

5

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19 March 2018

Masafumi Matsuo

6

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19 March 2018

Makoto Yoshino

7

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19 March 2018

Yosuke Shigematsu

8

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19 March 2018

Tohru Yorifuji

9

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19 March 2018

Mureo Kasahara

10

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19 March 2018

Fumio Endo

12

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19 March 2018

publication date

14 December 2011

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19 March 2018

Journal of Inherited Metabolic Disease

published in

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19 March 2018

volume

35

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19 March 2018

page(s)

777-785

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19 March 2018

issue

5

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19 March 2018

https://scigraph.springernature.com/pub.10.1007/s10545-011-9427-0

exact match

0 references

cites work

Long-term outcome of patients with urea cycle disorders and the question of neonatal screening

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https://api.crossref.org/works/10.1007%2FS10545-011-9427-0

Alternative pathway therapy for urea cycle disorders: twenty years later

21 January 2018

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Phenylacetylglutamine May Replace Urea as a Vehicle for Waste Nitrogen Excretion

21 January 2018

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New pathways of nitrogen excretion in inborn errors of urea synthesis

21 January 2018

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Alternative pathway therapy for urea cycle disorders.

21 January 2018

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https://api.crossref.org/works/10.1007%2FS10545-011-9427-0

Living-donor liver transplantation for carbamoyl phosphate synthetase 1 deficiency

21 January 2018

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The nutritional management of urea cycle disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10545-011-9427-0

Long-term treatment of girls with ornithine transcarbamylase deficiency

21 January 2018

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https://api.crossref.org/works/10.1007%2FS10545-011-9427-0

Current role of liver transplantation for the treatment of urea cycle disorders: a review of the worldwide English literature and 13 cases at Kyoto University

21 January 2018

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Neurologic outcome in children with inborn errors of urea synthesis. Outcome of urea-cycle enzymopathies.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10545-011-9427-0

Retrospective survey of urea cycle disorders: Part 2. Neurological outcome in forty-nine Japanese patients with urea cycle enzymopathies.

21 January 2018

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Urea cycle defects: management and outcome

21 January 2018

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Neurological outcome of patients with ornithine carbamoyltransferase deficiency

21 January 2018

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Current strategies for the management of neonatal urea cycle disorders

21 January 2018

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Liver transplantation for the treatment of urea cycle disorders

21 January 2018

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Coexistence of a graft with the preserved native liver in auxiliary partial orthotopic liver transplantation from a living donor for ornithine transcarbamylase deficiency

21 January 2018

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12 December 2020

Neurodevelopmental outcome of long-term therapy of urea cycle disorders in Japan

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12 December 2020

Dialysis in neonates with inborn errors of metabolism

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12 December 2020

Outcome and survival of 88 patients with urea cycle disorders: a retrospective evaluation

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12 December 2020

Ammonium-induced impairment of axonal growth is prevented through glial creatine.

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12 December 2020

Effects of arginine treatment on nutrition, growth and urea cycle function in seven Japanese boys with late-onset ornithine transcarbamylase deficiency

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12 December 2020

The ornithine transcarbamylase (OTC) gene: mutations in 50 Japanese families with OTC deficiency

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12 December 2020

Retrospective survey of urea cycle disorders: Part 1. Clinical and laboratory observations of thirty-two Japanese male patients with ornithine transcarbamylase deficiency

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12 December 2020

Estimated frequency of urea cycle enzymopathies in Japan

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12 December 2020

Long-term outcome of urea cycle disorders.

1 reference

12 December 2020

10.1007/S10545-011-9427-0

Identifiers

DOI

1 reference

19 March 2018

release_dmxphqseorc4zkdh7coejhy5be

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/dmxphqseorc4zkdh7coejhy5be

24 November 2022

mapped directly with Wikidata item

PubMed ID

22167275

1 reference

19 March 2018