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Results of search for 'su:"Glucosephosphate Dehydrogenase Deficiency"', page 32 of 236
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Authors
Bancone, Germana
Beutler, E
Boivin, P
Calabrese, E J
Cutillo, S
De Flora, A
Fiorelli, G
Fujii, H
Hammerman, C
Jacobasch, G
Kahn, A
Kaplan, M
Kaplan, Michael
Luzzatto, L
Meloni, T
Miwa, S
Morelli, A
Saha, N
Yoshida, A
el-Hazmi, M A
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Topics
Adolescent
Adult
Anemia, Hemolytic
Child
Child, Preschool
Erythrocytes
Female
Glucosephosphate Dehydrogenase
Glucosephosphate Dehydrogenase Deficiency
Humans
Infant, Newborn
Male
blood
complications
diagnosis
enzymology
epidemiology
etiology
genetics
metabolism
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621.
[Intraoperative intravascular hemolysis in a female patient with glucose-6-phosphate dehydrogenase deficiency].
[electronic resource]
by
Gimbert Burgos, E M
Díaz Fernández, J
López González, M C
Ruiz Marín, J J
Producer:
20020801
In:
Revista espanola de anestesiologia y reanimacion
vol. 48
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622.
[HEMOLYTIC ANEMIA CAUSED BY GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCY].
[electronic resource]
by
NEIMANN, N
PIERSON, M
Producer:
19961201
In:
La semaine des hopitaux : organe fonde par l'Association d'enseignement medical des hopitaux de Paris
vol. 39
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623.
GLUCOSE-6-PHOSPHATE DEHYDROGENASE (G6PD) DEFICIENCY, THALASSAEMIA, AND ABNORMAL HAEMOGLOBINS IN TAIWAN.
[electronic resource]
by
MOTULSKY, A G
LEE, T C
FRASER, G R
Producer:
19961201
In:
Journal of medical genetics
vol. 2
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624.
Haemolysis during diabetic ketoacidosis treatment in two girls with incomplete glucose-6-phosphate dehydrogenase deficiency.
[electronic resource]
by
Errico, Maria Katrin
Iovane, Brunella
Bernardini, Anna
Gliati, Dimitra
Scarabello, Chiara
Fainardi, Valentina
Chiari, Giovanni
Sav, Mario
Vanelli, Maurizio
Producer:
20091008
In:
Acta bio-medica : Atenei Parmensis
vol. 80
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625.
Case 3: Jaundice, Pallor, and Failure to Thrive in a 7-week-old Infant.
[electronic resource]
by
O'Brien, Brigid
Middleton, Brittany
Cua, Erica
Resnick, Alex
Ho, Cynthia H
Producer:
20180716
In:
Pediatrics in review
vol. 38
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626.
[G6PD deficiency in females with neonatal revelation. Report of four cases].
[electronic resource]
by
Renault, A
Mitanchez, D
Cortey, A
Producer:
20180615
In:
Archives de pediatrie : organe officiel de la Societe francaise de pediatrie
vol. 24
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627.
[Lipid aspects in subjects with glucose-6-phosphate dehydrogenase deficiency].
[electronic resource]
by
Addis, S
Meloni, M A
Producer:
19800226
In:
Bollettino della Societa italiana di biologia sperimentale
vol. 55
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628.
Treatment of leprosy.
[electronic resource]
by
Kulkarni, A G
Producer:
19930708
In:
The National medical journal of India
vol. 5
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629.
The suitability of saliva for detection of glucose-6-phosphate dehydrogenase deficiency.
[electronic resource]
by
Beamont, A H
Miguel, A
Goos, C M
Vermeesch-Markslag, A M
Hermans, A
Vermorken, A J
Producer:
19890317
In:
Molecular biology reports
vol. 13
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630.
[Current state of the diagnosis of hereditary hemoglobino- and enzymopathies].
[electronic resource]
by
Kovaleva, L G
Tokarev, Iu N
Erem'iants, A R
Tsibul'skaia, M M
Levina, A A
Producer:
19880128
In:
Gematologiia i transfuziologiia
vol. 32
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631.
Glucose-6-phosphate dehydrogenase deficiency and duodenal ulcer.
[electronic resource]
by
Addis, S
D'Ovidio, N
Producer:
19770812
In:
British medical journal
vol. 1
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632.
Glucose-6-phosphate dehydrogenase deficiency.
[electronic resource]
by
Jolly, J G
Producer:
19771229
In:
Journal of the Indian Medical Association
vol. 68
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633.
Study of erythrocyte glucose-6-phosphate dehydrogenase and abnormal haemoglobins in an endogamous community--"Katkaris"--a survey.
[electronic resource]
by
Kate, S L
Phadke, M A
Sainani, G S
Mutalik, G S
Producer:
19770512
In:
The Journal of the Association of Physicians of India
vol. 24
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634.
[Cytochemical study of erythrocyte glucose-6-phosphate dehydrogenase (G6PD) and its usefulness in the detection of a heterozygotic deficiency of G6PD].
[electronic resource]
by
Vives Corrons, J L
Merino, A
Pujades, M A
Producer:
19870115
In:
Sangre
vol. 31
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635.
Cancer genetic. 3. Genetic markers, childhood cancer problems.
[electronic resource]
by
Lynch, H T
Producer:
19740308
In:
The Nebraska medical journal
vol. 58
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636.
Spinal cord compression in homozygous beta thalassaemia.
[electronic resource]
by
Prabhakar, S
Chopra, J S
Khosla, V K
Dash, S
Banerjee, A K
Producer:
19800825
In:
Surgical neurology
vol. 13
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637.
[Spontaneous hemolysis in a patient with glucose-6-p-dehydrogenase deficiency (Mediterranean type) and heterozygote beta thalassemia].
[electronic resource]
by
Benöhr, H C
Usener, H
Wagner, H
Kleinhauer, E
Waller, H D
Producer:
19710204
In:
Die Medizinische Welt
vol. 24
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638.
[A case with XYY karyotype, Mediterranean disease and hypogammaglobulinemia].
[electronic resource]
by
Tannoia, N
Guanti, G
Trizio, D
Barsanti, P
Bonomo, L
Producer:
19710309
In:
Acta geneticae medicae et gemellologiae
vol. 19
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639.
[Hereditary blood diseases].
[electronic resource]
by
Ikkala, E
Producer:
19681016
In:
Duodecim; laaketieteellinen aikakauskirja
vol. 84
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640.
[Considerations on 2 cases of favism].
[electronic resource]
by
Schneer, J H
Schrotter, L
Crînganu, A
Producer:
19670722
In:
Medicina interna
vol. 18
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