GPI Mount Scopus — a variant of glucosephosphate isomerase deficiency
Author:
Publisher
Springer Science and Business Media LLC
Subject
Hematology,General Medicine
Link
http://link.springer.com/content/pdf/10.1007/BF01695868.pdf
Reference38 articles.
1. Arnold H (1979) Inherited glucosephosphate isomerase deficiency: a review of known variants and some aspects of the pathomechanism of the deficiency. Blut 39:405–417
2. Arnold H, Engelhardt R, Lohr GW, Jacobi H, Leibold I (1973) Glucosephosphat-Isomerase Typ Recklinghausen: eine neue Defektvariante mit hämolytischer Anämie. Klin Wochenschr 51:1198–1204
3. Arnold H, Dodinval-Versie J, Lambotte C, Lohr GW, van der Hofstadt J (1977) Glucosephosphate isomerase deficiency type Liege: a new variant with congenital nonspherocytic hemolytic anemia. Blut 35:187–193
4. Arnold H, Lohr GW, Hasslinger K, Podgajny T (1980) Augsburg-type glucosephosphate isomerase deficiency. Blut 40:107–115
5. Arnold H, Hasslinger K, Witt I (1983) Glucosephosphateisomerase type Kaiserlautern. A new variant causing congenital nonspherocytic hemolytic anemia. Blut 46:271–277
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1. Glucose 6 Phosphate Isomerase Deficiency, a Rare Hemolytic Anemia Misdiagnosed as Hereditary Spherocytosis;Journal of Pediatric Hematology/Oncology;2022-09-12
2. Hereditary nonspherocytic hemolytic anemia caused by glucose-6-phosphate isomerase (GPI) deficiency in a Chinese patient: a case report;BMC Pediatrics;2022-08-01
3. Attenuation of Hemolysis Due to Glucose-6-Phosphate Isomerase Deficiency With Ketogenic Diet – A Case Report;HemaSphere;2020-01-03
4. Hemolytic Anemia and Neurological Manifestations – An Uncommon Combination;The Indian Journal of Pediatrics;2019-06-10
5. Clinical and Molecular Spectrum of Glucose-6-Phosphate Isomerase Deficiency. Report of 12 New Cases;Frontiers in Physiology;2019-05-07
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