AAAAAA
Results: 1-25/30
Authors:
YALCIN SS
YURDAKOK K
OZALP I
COSKUN T
Citation: Ss. Yalcin et al., THE EFFECT OF LIVE MEASLES-VACCINES ON SERUM VITAMIN-A LEVELS IN HEALTHY-CHILDREN, Acta Paediatrica Japonica Overseas Edition, 40(4), 1998, pp. 345-349
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:
FRANCOIS B
PONZONE A
OZALP I
LEVY H
KAUFMAN E
ROMANO V
PUGLISIALLEGRA S
MCDONALD JD
Citation: B. Francois et al., PHENYLKETONURIA - FROM BIOCHEMISTRY TO TREATMENT - DISCUSSION, Journal of inherited metabolic disease, 21, 1998, pp. 20-52
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:
TANAKA K
GREGERSEN N
RIBES A
KIM J
KOLVRAA S
WINTER V
EIBERG H
MARTINEZ G
DEUFEL T
LEIFERT B
SANTER R
FRANCOIS B
PRONICKA E
LASZLO A
KMOCH S
KREMENSKY I
KALAYDJICVA L
OZALP I
ITO M
Citation: K. Tanaka et al., A SURVEY OF THE NEWBORN POPULATIONS IN BELGIUM, GERMANY, POLAND, CZECH-REPUBLIC, HUNGARY, BULGARIA, SPAIN, TURKEY, AND JAPAN FOR THE G985 VARIANT ALLELE WITH HAPLOTYPE ANALYSIS AT THE MEDIUM-CHAIN ACYL-COA DEHYDROGENASE GENE LOCUS - CLINICAL AND EVOLUTIONARY CONSIDERATION, Pediatric research, 41(2), 1997, pp. 201-209
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:
GURGEY A
OZALP I
ROTIG A
COSKUN T
TEKINALP G
ERDEM G
AKCOREN Z
CAGLAR M
BAKKALOGLU A
Citation: A. Gurgey et al., A CASE OF PEARSON SYNDROME-ASSOCIATED WITH MULTIPLE RENAL CYSTS, Pediatric nephrology, 10(5), 1996, pp. 637-638
Authors:
GUNGOR N
TOKATH A
COSKUN T
OZGUC M
OZALP I
Citation: N. Gungor et al., MICROCEPHALY IN A HYPERPHENYLALANINEMIC INFANT LEADING TO THE DIAGNOSIS OF MATERNAL HYPERPHENYLALANINEMIA, European journal of pediatrics, 155(3), 1996, pp. 257-258
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:
SALDAMLI I
KOKSEL H
OZBOY O
OZALP I
KILIC I
Citation: I. Saldamli et al., ZINC-SUPPLEMENTED BREAD AND ITS UTILIZATION IN ZINC-DEFICIENCY, Cereal chemistry, 73(4), 1996, pp. 424-427
Authors:
YORDAM N
CALIKOGLU AS
HATUN S
KANDEMIR N
OGUZ H
TEZIC T
OZALP I
Citation: N. Yordam et al., SCREENING FOR CONGENITAL HYPOTHYROIDISM IN TURKEY, European journal of pediatrics, 154(8), 1995, pp. 614-616
Authors:
SAHIN G
AYDIN A
ISIMER A
OZALP I
DURU S
Citation: G. Sahin et al., ALUMINUM CONTENT OF INFANT FORMULAS USED IN TURKEY, Biological trace element research, 50(1), 1995, pp. 87-96
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:
ARISOY AE
OZDEN S
CILIV G
OZALP I
Citation: Ae. Arisoy et al., TAY-SACHS-DISEASE - A CASE-REPORT, Turkish Journal of Pediatrics, 37(1), 1995, pp. 51-56
Authors:
TEKINALP G
COSKUN T
ORAN O
OZALP I
FIGEN G
ERGIN H
Citation: G. Tekinalp et al., NONKETOTIC HYPERGLYCINEMIA IN A NEWBORN-INFANT, Turkish Journal of Pediatrics, 37(1), 1995, pp. 57-60
Authors:
YILMAZ E
ERDEM H
OZGUC M
COSKUN T
OZCELIK U
GOCMEN A
OZALP I
Citation: E. Yilmaz et al., STUDY OF 12 MUTATIONS IN TURKISH CYSTIC-FIBROSIS PATIENTS, Human heredity, 45(3), 1995, pp. 175-177
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:
OZGUC M
YILMAZ E
ERDEM H
COSKUN T
OZCELIK U
TOGAN I
GOCMEN A
AYTER S
OZALP I
Citation: M. Ozguc et al., ALLELE FREQUENCIES OF MP6D-9 AND GATT MARKERS IN 32 TURKISH CYSTIC-FIBROSIS FAMILIES, Clinical genetics, 45(5), 1994, pp. 266-268
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