(Q38492042)

3 September 2017

Improved neutrophil function in a glycogen storage disease type 1b patient after liver transplantation (English)

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3 September 2017

liver transplantation

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inferred from title

glycogen storage disease

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1

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3 September 2017

4

Katsuhiko Tachibana

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3 September 2017

Masato Shinkai

2

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3 September 2017

Youkatsu Ohhama

3

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3 September 2017

Tadatoshi Kuratsuji

5

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3 September 2017

Hiroh Saji

6

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3 September 2017

Etsuko Maruya

7

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3 September 2017

11 February 2004

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European Journal of Pediatrics

3 September 2017

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3 September 2017

163

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3 September 2017

4-5

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3 September 2017

202-206

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https://scigraph.springernature.com/pub.10.1007/s00431-004-1405-1

3 September 2017

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cites work

Chemiluminescence probe with Cypridina luciferin analog, 2-methyl-6-phenyl-3,7-dihydroimidazo[1,2-a]pyrazin-3-one, for estimating the ability of human granulocytes to generate O2-

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12 December 2020

Glycogen storage disease type Ib without neutropenia.

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12 December 2020

Liver transplantation for type Ib glycogenosis with reversal of cyclic neutropenia

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12 December 2020

Inhibition of microsomal glucose-6-phosphate transport in human neutrophils results in apoptosis: a potential explanation for neutrophil dysfunction in glycogen storage disease type 1b.

1 reference

12 December 2020

Genetic basis of glycogen storage disease type 1a: prevalent mutations at the glucose-6-phosphatase locus

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12 December 2020

Treatment with lenograstim (glycosylated recombinant human granulocyte colony-stimulating factor) and orthotopic liver transplantation for glycogen storage disease type Ib

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12 December 2020

Chimerism after liver transplantation for type IV glycogen storage disease and type 1 Gaucher's disease

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12 December 2020

Amount of co-transplanted donor-derived leukocytes determines in-vivo microchimerism and mixed lymphocyte culture changes post-liver transplantation

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12 December 2020

Glucose-6-phosphatase mutation G188R confers an atypical glycogen storage disease type 1b phenotype

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12 December 2020

Brief report: treatment of chronic inflammatory bowel disease in glycogen storage disease type Ib with colony-stimulating factors

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12 December 2020

In vivo effects of recombinant human granulocyte colony-stimulating factor on normal neutrophil function and membrane effector molecule expression

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12 December 2020

Molecular analysis of glycogen storage disease type Ib: identification of a prevalent mutation among Japanese patients and assignment of a putative glucose-6-phosphate translocase gene to chromosome 11

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12 December 2020

Flow cytometric studies of oxidative product formation by neutrophils: a graded response to membrane stimulation.

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12 December 2020

Liver transplantation for glycogen storage disease types I, III, and IV

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12 December 2020

Granulocyte colony-stimulating factor in glycogen storage disease type 1b. Results of the European Study on Glycogen Storage Disease Type 1

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12 December 2020

A gene on chromosome 11q23 coding for a putative glucose- 6-phosphate translocase is mutated in glycogen-storage disease types Ib and Ic.

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12 December 2020

Inactivation of the glucose 6-phosphate transporter causes glycogen storage disease type 1b.

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12 December 2020

Quantitation of neutrophil phagocytosis, using fluorescent latex beads. Correlation of microscopy and flow cytometry

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12 December 2020

Glycogen storage disease type Ib: structural and mutational analysis of the microsomal glucose-6-phosphate transporter gene

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12 December 2020

The first cooperative living-related donor liver transplantation performed by two separate institution teams: The Kanagawa Liver Transplantation Program

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12 December 2020

Superoxide anion production and expression of cytochrome b 558 by neutrophils are impaired in some patients with myelodysplastic syndrome

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12 December 2020

Historical highlights and unsolved problems in glycogen storage disease type 1.

1 reference

12 December 2020

10.1007/S00431-004-1405-1

Identifiers

DOI

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Dimensions Publication ID

3 September 2017

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