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Biotinidase deficiency with neurological features resembling multiple sclerosis

Journal of inherited metabolic disease, 1997-09, Vol.20 (5), p.707-708

1997

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Mutational analysis of Turkish galactosaemia patients

Journal of inherited metabolic disease, 1995-05, Vol.18 (3), p.368-369

1995

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Genetic and neurological evaluation of untreated and late‐treated patients with phenylketonuria

Journal of inherited metabolic disease, 1994-05, Vol.17 (3), p.371-371

1994

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Association between mutations and the variable number tandem repeat alleles in a sample of Turkish phenylketonuria patients

Journal of inherited metabolic disease, 1994-05, Vol.17 (3), p.373-374

1994

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Heterozygous carriers of classical phenylketonuria in a sample of the turkish population: Detection by a spectrofluorimetric method

Journal of inherited metabolic disease, 1991-09, Vol.14 (5), p.741-748

1991

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Maple syrup urine disease: Mutation analysis in Turkish patients

Journal of inherited metabolic disease, 2002-05, Vol.25 (2), p.89-97

2002

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Molecular basis of mild hyperphenylalaninaemia in Turkey

Journal of inherited metabolic disease, 2000-07, Vol.23 (5), p.523-525

2000

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PP-109 CHROMATIN MODIFICATION GENES PLAY PIVOTAL ROLE IN BORTEZOMIB INDUCED GROWTH SUPPRESSION IN CHRONIC MYELOID LEUKEMIA

Leukemia research, 2014-10, Vol.38, p.S61-S61

2014

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Molecular analysis of 16 Turkish families with DHPR deficiency using denaturing gradient gel electrophoresis (DGGE)

Human genetics, 2000-12, Vol.107 (6), p.546-553

2000

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Zinc-supplemented bread and its utilization in zinc deficiency

Cereal chemistry, 1996-07, Vol.73 (4), p.424-427

1996

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The Effect of Zinc-Supplemented Bread Consumption on School Children with Asymptomatic Zinc Deficiency

Journal of pediatric gastroenterology and nutrition, 1998-02, Vol.26 (2), p.167-171

1998

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A case of Pearson syndrome associated with multiple renal cysts

Pediatric nephrology (Berlin, West), 1996-10, Vol.10 (5), p.637-638

1996

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Fifteen years' experience with 212 hyperammonaemic cases at a Metabolic Unit

Journal of inherited metabolic disease, 1991-09, Vol.14 (5), p.698-706

1991

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Study of 12 mutations in Turkish cystic fibrosis patients

Human heredity, 1995, Vol.45 (3), p.175

1995

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The major presenting symptom in a biotinidase‐deficient patient: Laryngeal stridor

Journal of inherited metabolic disease, 1992-03, Vol.15 (2), p.281-282

1992

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Investigation of serum vitamin A levels of children who had a history of recurrent diarrhoea and acute respiratory infections in Ankara

Journal of tropical pediatrics (1980), 1990-10, Vol.36 (5), p.251-255

1990

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3‐Hydroxy‐3‐methylglutaryl coenzyme A lyase deficiency

Journal of inherited metabolic disease, 1993-11, Vol.16 (6), p.1062-1063

1993

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Scleroderma-like skin lesions in two patients with phenylketonuria

European journal of pediatrics, 1990-12, Vol.150 (2), p.109-110

1990

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Hyperphenylalaninaemia due to tetrahydrobiopterin deficiency: A report of 16 cases

Journal of inherited metabolic disease, 1993-05, Vol.16 (3), p.605-607

1993

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Aluminum content of infant formulas used in Turkey

Biological trace element research, 1995-10, Vol.50 (1), p.87-96

1995

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Dermatoglyphic study in children with phenylketonuria

Journal of inherited metabolic disease, 1989-09, Vol.12 (3), p.323-326

1989

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Phenylketonuria in turkey: Experience with an enzymatic colorimetric test for measurement of serum phenylalanine

Journal of inherited metabolic disease, 1990-01, Vol.13 (3), p.295-297

1990

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Allele frequencies of Mp6D-9 and GATT markers in 32 Turkish cystic fibrosis families

Clinical genetics, 1994-05, Vol.45 (5), p.266-268

1994

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Novel mutations cause biotinidase deficiency in Turkish children

Journal of inherited metabolic disease, 2000-03, Vol.23 (2), p.120-128

2000

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Lethal hyperammonaemic coma due to ornithine transcarbamylase deficiency presenting as brain stem encephalitis in a previously asymptomatic ten‐year‐old boy

Journal of inherited metabolic disease, 1987-09, Vol.10 (3), p.271-271

1987

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Biotinidase deficiency with neurological features resembling multiple sclerosis

Mutational analysis of Turkish galactosaemia patients

Genetic and neurological evaluation of untreated and late‐treated patients with phenylketonuria

Association between mutations and the variable number tandem repeat alleles in a sample of Turkish phenylketonuria patients

Heterozygous carriers of classical phenylketonuria in a sample of the turkish population: Detection by a spectrofluorimetric method

Maple syrup urine disease: Mutation analysis in Turkish patients

Molecular basis of mild hyperphenylalaninaemia in Turkey

PP-109 CHROMATIN MODIFICATION GENES PLAY PIVOTAL ROLE IN BORTEZOMIB INDUCED GROWTH SUPPRESSION IN CHRONIC MYELOID LEUKEMIA

Molecular analysis of 16 Turkish families with DHPR deficiency using denaturing gradient gel electrophoresis (DGGE)

Zinc-supplemented bread and its utilization in zinc deficiency

The Effect of Zinc-Supplemented Bread Consumption on School Children with Asymptomatic Zinc Deficiency

A case of Pearson syndrome associated with multiple renal cysts

Fifteen years' experience with 212 hyperammonaemic cases at a Metabolic Unit

Study of 12 mutations in Turkish cystic fibrosis patients

The major presenting symptom in a biotinidase‐deficient patient: Laryngeal stridor

Investigation of serum vitamin A levels of children who had a history of recurrent diarrhoea and acute respiratory infections in Ankara

3‐Hydroxy‐3‐methylglutaryl coenzyme A lyase deficiency

Scleroderma-like skin lesions in two patients with phenylketonuria

Hyperphenylalaninaemia due to tetrahydrobiopterin deficiency: A report of 16 cases

Aluminum content of infant formulas used in Turkey

Dermatoglyphic study in children with phenylketonuria

Phenylketonuria in turkey: Experience with an enzymatic colorimetric test for measurement of serum phenylalanine

Allele frequencies of Mp6D-9 and GATT markers in 32 Turkish cystic fibrosis families

Novel mutations cause biotinidase deficiency in Turkish children

Lethal hyperammonaemic coma due to ornithine transcarbamylase deficiency presenting as brain stem encephalitis in a previously asymptomatic ten‐year‐old boy

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