AAAAAA
Results:
1-16
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Results: 16
Authors:
KILIC L
OZALP I
COSKUN T
TOKATLI A
EMRE S
SALDAMLI I
KOKSEL H
OZBOY O
Citation: L. Kilic et al., THE EFFECT OF ZINC-SUPPLEMENTED BREAD CONSUMPTION ON SCHOOL-CHILDREN WITH ASYMPTOMATIC ZINC-DEFICIENCY, Journal of pediatric gastroenterology and nutrition, 26(2), 1998, pp. 167-171
Authors:
WOLF B
POMPONIO RJ
NORRGARD KJ
LOTT IT
BAUMGARTNER ER
SUORMALA T
RAMAEKERS VT
COSKUN T
TOKATLI A
OZALP I
HYMES J
Citation: B. Wolf et al., DELAYED-ONSET PROFOUND BIOTINIDASE DEFICIENCY, The Journal of pediatrics, 132(2), 1998, pp. 362-365
Authors:
TOKATLI A
COSKUN T
OZALP I
Citation: A. Tokatli et al., BIOTINIDASE DEFICIENCY WITH NEUROLOGICAL FEATURES RESEMBLING MULTIPLE-SCLEROSIS, Journal of inherited metabolic disease, 20(5), 1997, pp. 707-708
Authors:
TOKATLI A
COSKUN T
OZALP I
Citation: A. Tokatli et al., HYPOPHOSPHATEMIC VITAMIN-D-RESISTANT RICKETS ASSOCIATED WITH EPIDERMAL NEVUS SYNDROME - A CASE-REPORT, Turkish Journal of Pediatrics, 39(2), 1997, pp. 247-251
Authors:
CAKMAK FN
AYAZ HE
ERGUL P
ALIEFENDIOGLU D
TOKATLI A
COSKUN T
OZALP I
Citation: Fn. Cakmak et al., MATERNAL SCREENING FOR PHENYLKETONURIA DURING REPRODUCTIVE AGE, Journal of investigative medicine, 44(1), 1996, pp. 188-188
Authors:
GUNGOR N
TOKATLI A
COSKUN T
OZGUC M
OZALP I
Citation: N. Gungor et al., MICROCEPHALY AND MATERNAL PHENYLKETONURIA - REPLY, European journal of pediatrics, 155(11), 1996, pp. 992-992
Authors:
COSKUN T
ERKUL E
SEYRANTEPE V
OZGUC M
TOKATLI A
OZALP I
Citation: T. Coskun et al., MUTATIONAL ANALYSIS OF TURKISH GALACTOSEMIA PATIENTS, Journal of inherited metabolic disease, 18(3), 1995, pp. 368-369
Authors:
OZALP I
COSKUN T
OZGUC M
TOKATLI A
YALAZ K
VANLI L
YILMAZ E
ERBAY A
Citation: I. Ozalp et al., GENETIC AND NEUROLOGICAL EVALUATION OF UNTREATED AND LATE-TREATED PATIENTS WITH PHENYLKETONURIA, Journal of inherited metabolic disease, 17(3), 1994, pp. 371-371
Authors:
OZGUC M
YILMAZ E
ERDEM H
COSKUN T
TOKATLI A
OZALP I
Citation: M. Ozguc et al., ASSOCIATION BETWEEN MUTATIONS AND THE VARIABLE NUMBER TANDEM REPEAT ALLELES IN A SAMPLE OF TURKISH PHENYLKETONURIA PATIENTS, Journal of inherited metabolic disease, 17(3), 1994, pp. 373-374
Authors:
COSKUN T
TOKATLI A
OZALP I
Citation: T. Coskun et al., INBORN-ERRORS OF BIOTIN METABOLISM - CLINICAL AND LABORATORY FEATURESOF 8 CASES, Turkish Journal of Pediatrics, 36(4), 1994, pp. 267-278
Authors:
TOKATLI A
COSKUN T
KOCABAS CN
OZALP I
BALCI S
Citation: A. Tokatli et al., CLASSICAL PHENYLKETONURIA ASSOCIATED WITH GOLDENHARS-SYNDROME - A CASE-REPORT, Turkish Journal of Pediatrics, 36(2), 1994, pp. 153-156
Authors:
KALAYCI O
COSKUN T
TOKATLI A
DEMIR E
ERDEM G
GUNGOR C
YUKSELEN A
OZALP I
Citation: O. Kalayci et al., INFANTILE SPASMS AS THE INITIAL SYMPTOM OF BIOTINIDASE DEFICIENCY, The Journal of pediatrics, 124(1), 1994, pp. 103-104
Authors:
GUNEL M
COSKUN T
TOKATLI A
OZALP I
Citation: M. Gunel et al., 3-HYDROXY-3-METHYLGLUTARYL COENZYME-A LYASE DEFICIENCY, Journal of inherited metabolic disease, 16(6), 1993, pp. 1062-1063
Authors:
COSKUN T
OZALP I
TOKATLI A
BLAU N
NIEDERWIESER A
Citation: T. Coskun et al., HYPERPHENYLALANINEMIA DUE TO TETRAHYDROBIOPTERIN DEFICIENCY - A REPORT OF 16 CASES, Journal of inherited metabolic disease, 16(3), 1993, pp. 605-607
Authors:
TOKATLI A
OZSOYLU S
OZME S
Citation: A. Tokatli et al., LEPRECHAUNISM (DONOHUES SYNDROME) - A CASE-REPORT, Turkish Journal of Pediatrics, 35(4), 1993, pp. 319-322
Authors:
COSKUN T
OZALP I
TOKATLI A
Citation: T. Coskun et al., IMINOGLYCINURIA - A BENIGN TYPE OF INHERITED AMINOACIDURIA, Turkish Journal of Pediatrics, 35(2), 1993, pp. 121-125
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1-16
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