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TOPALOGLU H
TALIM B
VIGNIER N
HELBLINGLECLERC A
YETUK M
AFSIN IE
CAGLAR M
KALE G
GUICHENEY P
Citation: H. Topaloglu et al., MEROSIN-DEFICIENT CONGENITAL MUSCULAR-DYSTROPHY WITH SEVERE MENTAL-RETARDATION AND NORMAL CRANIAL MRI - A REPORT OF 2 SIBLINGS, Neuromuscular disorders, 8(3-4), 1998, pp. 169-174
Authors:
PEKSOY I
CANER B
KALE G
AKCOREN Z
BEKDIK CF
Citation: I. Peksoy et al., TC-99M PERTECHNETATE SCINTIGRAPHY FOR THE DETECTION OF ILEAL DUPLICATION, Clinical nuclear medicine, 23(4), 1998, pp. 233-234
Authors:
OZCELIK U
OZKARA HA
GOCMEN A
AKCOREN Z
KOCAGOZ T
KIPER N
GOGUS S
CAGLAR M
KALE G
KOTILOGLU E
Citation: U. Ozcelik et al., DETECTION OF MYCOBACTERIUM-TUBERCULOSIS DNA IN TISSUE SAMPLES OF CHILDREN WITH SARCOIDOSIS, Pediatric pulmonology, 24(2), 1997, pp. 122-124
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BALCI S
BEKSAC S
AKTAS D
BODUROGLU K
KALE G
ERCAL D
ONO B
Citation: S. Balci et al., AN UNUSUAL FAMILIAL CHROMOSOMAL TRANSLOCATION IN BOTH PARENTS - MOTHER 45,XX,T(14Q-21Q), FATHER 46,XY,T(1-4)(P36,1-P14) - RESULTS OF 10 CONSECUTIVE PREGNANCIES WITH CLINICAL, CYTOGENETIC AND POSTMORTEM FINDINGS, Cytogenetics and cell genetics, 77(1-2), 1997, pp. 137-137
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KOCAK N
GURAKAN F
YUCE A
CAGLAR M
KALE G
GOGUS S
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ANDIRAN F
TANYEL FC
KALE G
AKHAN O
AKCOREN Z
HICSONMEZ A
Citation: F. Andiran et al., OBSTRUCTIVE-JAUNDICE RESULTING FROM ADENOCARCINOMA OF THE AMPULLA OF VATER IN AN 11-YEAR-OLD BOY, Journal of pediatric surgery, 32(4), 1997, pp. 636-637
Authors:
TEZCAN I
DEMIR E
ASAN E
KALE G
MUFTUOGLU SF
KOTILOGLU E
Citation: I. Tezcan et al., A NEW CASE OF OCULOCEREBRAL HYPOPIGMENTATION SYNDROME (CROSS SYNDROME) WITH ADDITIONAL FINDINGS, Clinical genetics, 51(2), 1997, pp. 118-121
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TASDEMIR HA
KOTILOGLU E
TOPALOGLU H
KALE G
DINCER DP
YALAZ K
RENDA Y
Citation: Ha. Tasdemir et al., FUNCTIONAL-SIGNIFICANCE OF DYSTROPHIN-POSITIVE FIBERS IN DUCHENNE ANDBECKER MUSCULAR-DYSTROPHY, PEDIATRIC PATHOLOGY & LABORATORY MEDICINE, 16(4), 1996, pp. 583-590
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OZDEMIR S
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BAKKALOGLU A
KOTILOGLU E
KALE G
Citation: U. Saatci et al., LATE CARDIAC AND VASCULAR COMPLICATIONS OF PRIMARY HYPEROXALURIA IN CHILDHOOD, Pediatric nephrology, 10(5), 1996, pp. 677-678
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KALE G
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BERBEROGLU S
BUYUKPAMUKCU N
SARIALIOGLU F
KALE G
AKYUZ C
KUTLUK T
Citation: M. Buyukpamukcu et al., NONLYMPHOID GASTROINTESTINAL MALIGNANCIES IN TURKISH CHILDREN, Medical and pediatric oncology, 26(1), 1996, pp. 28-35
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Authors:
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YUCE A
GURAKAN F
OZEN H
GOGUS S
KALE G
CAGLAR M
Citation: N. Kocak et al., COLCHICINE IN THE TREATMENT OF HEPATIC-FIBROSIS IN CHILDREN, The American journal of gastroenterology, 91(1), 1996, pp. 179-180
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ORAN O
KOTILOGLU E
KALE G
TOPCU M
RENDA Y
Citation: G. Erdem et al., INTESTINAL LYMPHANGIECTASIA IN A PATIENT WITH ZELLWEGER CEREBROHEPATORENAL SYNDROME, American journal of medical genetics, 58(2), 1995, pp. 152-154
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SENOCAK ME
KOTILOGLU E
KALE G
HICSONMEZ A
Citation: A. Turken et al., SOLITARY INTESTINAL FIBROMATOSIS MIMICKING MALABSORPTION-SYNDROMES, Journal of pediatric surgery, 30(9), 1995, pp. 1387-1389
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SAYLI T
GUNAY M
ERSOY F
KUCUKALI T
KALE G
CAGLAR M
Citation: A. Gurgey et al., HIGH-DOSE METHYLPREDNISOLONE AND VP-16 IN TREATMENT OF GRISCELLI SYNDROME WITH CENTRAL-NERVOUS-SYSTEM INVOLVEMENT, American journal of hematology, 47(4), 1994, pp. 331-332
Authors:
TOPALOGLU H
KALE G
YALNIZOGLU D
TASDEMIR AH
KARADUMAN A
TOPCU M
KOTILOGLU E
Citation: H. Topaloglu et al., ANALYSIS OF PURE CONGENITAL MUSCULAR-DYSTROPHIES IN 38 CASES - HOW DIFFERENT IS THE CLASSICAL TYPE-1 FROM THE OCCIDENTAL TYPE CEREBROMUSCULAR DYSTROPHY, Neuropediatrics, 25(2), 1994, pp. 94-100