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Citations to this article

Impaired carbohydrate metabolism of polymorphonuclear leukocytes in glycogen storage disease Ib.
N Bashan, … , R Potashnik, S W Moses
N Bashan, … , R Potashnik, S W Moses
Published May 1, 1988
Citation Information: J Clin Invest. 1988;81(5):1317-1322. https://doi.org/10.1172/JCI113457.
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Research Article

Impaired carbohydrate metabolism of polymorphonuclear leukocytes in glycogen storage disease Ib.

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Abstract

This study measures hexose monophosphate (HMP) shunt activity, glycolytic rate, and glucose transport in PMN and lymphocytes of patients with glycogen storage disease (GSD) type Ib as compared with controls and with GSD Ia patients. HMP shunt activity and glycolysis were significantly lower in intact PMN cells of GSD Ib patients as compared with GSD Ia patients and with controls. These activities were above normal levels in disrupted GSD Ib PMN. HMP shunt activity and glycolytic rates in lymphocytes were similar in all three groups studied. The rate of 2-deoxyglucose transport into GSD Ib PMN was 30% of that into cells of normal controls. In GSD Ib lymphocytes or in GSD Ia PMN and lymphocytes transport was normal. The striking limitation of glucose transport across the cell membrane of the PMN of GSD Ib patients may account for the impairment of leukocyte function that is characteristic of GSD Ib, but not found in GSD Ia patients.

Authors

N Bashan, Y Hagai, R Potashnik, S W Moses

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Total citations by year

Year: 2011 2010 2005 2003 2002 2001 2000 1999 1998 1996 1994 1993 1992 1991 1990 1989 Total
Citations: 1 1 3 1 2 1 2 1 1 1 1 3 1 3 3 1 26
Citation information
This citation data is accumulated from CrossRef, which receives citation information from participating publishers, including this journal. Not all publishers participate in CrossRef, so this information is not comprehensive. Additionally, data may not reflect the most current citations to this article, and the data may differ from citation information available from other sources (for example, Google Scholar, Web of Science, and Scopus).

Citations to this article (26)

Title and authors Publication Year
G6PC3 mutations are associated with a major defect of glycosylation: a novel mechanism for neutrophil dysfunction
B Hayee, A Antonopoulos, EJ Murphy, FZ Rahman, G Sewell, BN Smith, S McCartney, M Furman, G Hall, SL Bloom, SM Haslam, HR Morris, K Boztug, C Klein, B Winchester, E Pick, DC Linch, RE Gale, AM Smith, A Dell, AW Segal
Glycobiology 2011
Long term G-CSF-induced remission of ulcerative colitis-like inflammatory bowel disease in a patient with glycogen storage disease Ib and evaluation of associated neutrophil function
A Alsultan, RJ Sokol, MA Lovell, G Thurman, DR Ambruso
Pediatric Blood & Cancer 2010
Unusual Oral Manifestations and Evolution in Glycogen Storage Disease Type Ib
C Mortellaro, U Garagiola, V Carbone, F Cerutti, V Marci, PL Bonda
Journal of Craniofacial Surgery 2005
Amelioration of Neutrophil Membrane Function Underlies Granulocyte-Colony Stimulating Factor Action in Glycogen Storage Disease 1b
E Lesma, E Riva, M Giovannini, AM Giulio, A Gorio
International journal of immunopathology and pharmacology 2005
Atlas of Metabolic Diseases Second edition
W Nyhan, B Barshop, P Ozand
Atlas of Metabolic Diseases Second edition 2005
Membrane Transporter Diseases
S Bröer, CA Wagner
2003
Association of glycogen storage disease 1b and Crohn disease: results of a North American survey
BK Dieckgraefe, JR Korzenik, A Husain, L Dieruf
European Journal of Pediatrics 2002
The glucose-6-phosphatase system
E Schaftingen, I Gerin
Biochemical Journal 2002
Granulocyte–Macrophage Colony-Stimulating Factor for Treating Gastrostomy Tube Site Healing in a Child With Glycogen Storage Disease Type Ib
BA Steinmetz, MG Martin, RL Roberts
Journal of Pediatric Gastroenterology and Nutrition 2001
Glucose-6-Phosphatase Mutation G188R Confers an Atypical Glycogen Storage Disease Type 1b Phenotype
BW Weston, JL Lin, J Muenzer, HS Cameron, RR Arnold, HH Seydewitz, E Mayatepek, EV Schaftingen, M Veiga-Da-Cunha, D Matern, YT Chen
Pediatric Research 2000
Neutropenia, neutrophil dysfunction, and inflammatory bowel disease in glycogen storage disease type Ib: Results of the European Study on Glycogen Storage Disease Type I
G Visser, JP Rake, J Fernandes, P Labrune, JV Leonard, S Moses, K Ullrich, GP Smit
The Journal of Pediatrics 2000
A Convenient Diagnostic Function Test of Peripheral Blood Neutrophils in Glycogen Storage Disease Type Ib
AJ Verhoeven, G Visser, RV Zwieten, B Gruszczynska, DW Poll-The, GP Smit
Pediatric Research 1999
Principles of Perinatal—Neonatal Metabolism
RM Cowett
1998
Treatment of Chronic Enteritis in Glycogen Storage Disease Type IB with Granulocyte Colny-Stimulating Factor
EG Hoover, JJ DuBois, TL Samples, JS McCullough, PJ Chenaille, RG Montes
Journal of Pediatric Gastroenterology &amp Nutrition 1996
Postnatal regression of glucose transport in a patient with glycogen storage disease type 1b
J Levy, MT Abu-Ras, T Berenstein, R Potashnik, I Meisner, SW Moses, N Bashan
Journal of Inherited Metabolic Disease 1994
Defective neutrophil and monocyte functions in glycogen storage disease type Ib: A literature review
R Gitzelmann, NU Bosshard
European Journal of Pediatrics 1993
Deficient glucose phosphorylation as a possible common denominator and its relation to abnormal leucocyte function, in glycogen storage disease 1b patients
N Bashan, R Potashnik, A Peist, N Peleg, A Moran, SW Moses
European Journal of Pediatrics 1993
Impairment of calcium mobilization in phagocytic cells in glycogen storage disease type 1b
HM Korchak, , CA Stanley, L Baker, SD Douglas, L Kilpatrick
European Journal of Pediatrics 1993
Brain abscesses in glycogen-storage disease-type 1b
BZ Garty, A Rachmel, H Mandel, M Nitzan
Acta Paediatrica 1992
Chronic inflammatory bowel disease in glycogen storage disease type 1B
IR Sanderson, WM Bisset, PJ Milla, JV Leonard
Journal of Inherited Metabolic Disease 1991
Brain Abscess in Glycogen Storage Disease Type Ib
HK Park, SG Kahler, YT Chen
Acta Paediatrica 1991
Granulocyte and granulocyte-macrophage colony-stimulating factors for treatment of neutropenia in glycogen storage disease type Ib
H Schroten, J Roesler, T Breidenbach, U Wendel, J Elsner, S Schweitzer, C Zeidler, S Burdach, ML Lohmann-Matthes, V Wahn, K Welte
The Journal of Pediatrics 1991
Impaired metabolic function and signaling defects in phagocytic cells in glycogen storage disease type 1b
L Kilpatrick, BZ Garty, KF Lundquist, K Hunter, CA Stanley, L Baker, SD Douglas, HM Korchak
Journal of Clinical Investigation 1990
Uptake and transport of hexoses into polymorphonuclear leukocytes of patients with glycogen storage disease type 1b
N Bashan, R Potashnik, N Peleg, A Moran, SW Moses
Journal of Inherited Metabolic Disease 1990
Normal polymorphonuclear neutrophil function in a case of glycogen storage disease type Ib
E Bonioli, C Bellini, AD Stefano, A Costa, S Canini, F Patrone
European Journal of Pediatrics 1990
A Method for the Diagnosis of Glycogen Storage Disease Type Ib using Polymorphonuclear Leukocytes
N Bashan, R Potashnik, M Phillip, YS Shin, SW Moses
Journal of Inherited Metabolic Disease 1989

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