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Results: 1-11 |
Results: 11
RECOMBINANT ALPHA-2A INTERFERON TREATMENT IN A CHILD WITH T-CELL LEUKEMIA AND CHRONIC HEPATITIS-B
Authors: OREN H DUZOVALI O IRKEN G
Citation: H. Oren et al., RECOMBINANT ALPHA-2A INTERFERON TREATMENT IN A CHILD WITH T-CELL LEUKEMIA AND CHRONIC HEPATITIS-B, Annals of hematology, 77(4), 1998, pp. 187-190
INHIBITOR DEVELOPMENT IN HEMOPHILIA PATIENTS
Authors: OREN H YAPRAK I DEVECI C IRKEN G
Citation: H. Oren et al., INHIBITOR DEVELOPMENT IN HEMOPHILIA PATIENTS, British Journal of Haematology, 102(1), 1998, pp. 136-136
PLATELET ACTIVATION DURING THE EARLY NEONATAL-PERIOD
Authors: IRKEN G UYSAL KM OLGUN N UNDAR B AKKOC N OZKAN H AKYOL F CEVIK NT
Citation: G. Irken et al., PLATELET ACTIVATION DURING THE EARLY NEONATAL-PERIOD, Biology of the neonate, 73(3), 1998, pp. 166-171
PLATELET ACTIVATION IN CONGENITAL HEART-DISEASES
Authors: OLGUN N UYSAL KM IRKEN G UNAL N UNDAR B AKKOC N AKCORAL A SARIALIOGLU F CEVIK N
Citation: N. Olgun et al., PLATELET ACTIVATION IN CONGENITAL HEART-DISEASES, Acta Paediatrica Japonica Overseas Edition, 39(5), 1997, pp. 566-569
COMPOUND HETEROZYGOSITY FOR HEMOGLOBIN KNOSSOS [ALPHA(2)BETA(2)-27-(B9)-ALA-SER] AND IVS I-1 MUTATION
Authors: GURGEY A BALKAN H IRKEN G GUMRUK F ALTAY S KALAYCIOGLU A ONER C ONER R
Citation: A. Gurgey et al., COMPOUND HETEROZYGOSITY FOR HEMOGLOBIN KNOSSOS [ALPHA(2)BETA(2)-27-(B9)-ALA-SER] AND IVS I-1 MUTATION, Turkish Journal of Pediatrics, 39(2), 1997, pp. 253-257
CONGENITAL HYPOPLASTIC-ANEMIA IN 6 PATIENTS - UNUSUAL ASSOCIATION OF SHORT PROXIMAL PHALANGES WITH MILD ANEMIA
Authors: CETIN M KARA A GURGEY A GUMRUK F IRKEN G YETGIN S ALTAY C
Citation: M. Cetin et al., CONGENITAL HYPOPLASTIC-ANEMIA IN 6 PATIENTS - UNUSUAL ASSOCIATION OF SHORT PROXIMAL PHALANGES WITH MILD ANEMIA, Pediatric hematology and oncology, 12(2), 1995, pp. 153-158
FAMILIAL SELECTIVE VITAMIN-B12 MALABSORPTION (IMERSLUND-GRASBECK SYNDROME) IN A POOL OF TURKISH PATIENTS
Authors: ALTAY C CETIN M GUMRUK F IRKEN G YETGIN S LALELI Y
Citation: C. Altay et al., FAMILIAL SELECTIVE VITAMIN-B12 MALABSORPTION (IMERSLUND-GRASBECK SYNDROME) IN A POOL OF TURKISH PATIENTS, Pediatric hematology and oncology, 12(1), 1995, pp. 19-28
RELATIONSHIP BETWEEN SERUM UNCONJUGATED BILIRUBIN LEVELS AND THE AUTOFLUORESCENCE OF WHITE BLOOD-CELLS IN NEONATAL JAUNDICE
Authors: OZKAN H AKKOC N AYDIN A KAVUKCU S OLGUN N IRKEN G AKYOL F CEVIK NT
Citation: H. Ozkan et al., RELATIONSHIP BETWEEN SERUM UNCONJUGATED BILIRUBIN LEVELS AND THE AUTOFLUORESCENCE OF WHITE BLOOD-CELLS IN NEONATAL JAUNDICE, Biology of the neonate, 68(2), 1995, pp. 100-103
AASE-SMITH SYNDROME - REPORT OF A NEW CASE WITH UNUSUAL FEATURES
Authors: YETGIN S BALCI S IRKEN G COSKUN T SAY B
Citation: S. Yetgin et al., AASE-SMITH SYNDROME - REPORT OF A NEW CASE WITH UNUSUAL FEATURES, Turkish Journal of Pediatrics, 36(3), 1994, pp. 239-242
DIFFUSE ERYTHRODERMIC CUTANEOUS MASTOCYTOSIS WITH BONE-MARROW INFILTRATION
Authors: OLGUN N OREN H OREN B IRKEN G POLAT M CEVIK N
Citation: N. Olgun et al., DIFFUSE ERYTHRODERMIC CUTANEOUS MASTOCYTOSIS WITH BONE-MARROW INFILTRATION, Dermatology, 187(2), 1993, pp. 127-129
PELGER-HUET ANOMALY WITH TRISOMY-18-SYNDROME
Authors: IRKEN G OLGUN N OREN H OREN B CEVIK N SAKIZLI M
Citation: G. Irken et al., PELGER-HUET ANOMALY WITH TRISOMY-18-SYNDROME, American journal of hematology, 43(4), 1993, pp. 328-329
Risultati: 1-11 |