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Equilibrium Efficiency Improvement in MIMO Interference Systems: A Decentralized Stream Control Approach

IEEE transactions on wireless communications, 2007-08, Vol.6 (8), p.2984-2993

2007

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Evaluation of the angulation of the nasal septum deviation as an anatomical variation for increased frequency of antral pseudocyst: a cone-beam computed tomography study

Folia morphologica, 2023-01, Vol.82 (1), p.158-165

2023

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Combined antihypertensive treatment is better than mono-therapy in hypertensive patients

Netherlands journal of medicine, 2020-09, Vol.78 (5), p.239-243

2020

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Follow up of phenylketonuria patients

Molecular genetics and metabolism, 2011, Vol.104, p.S31-S39

2011

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A novel catalyst for diesel soot oxidation

Applied catalysis. B, Environmental, 2005-11, Vol.61 (3-4), p.334-345

2005

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Effects of low-level laser therapy on osteoblastic bone formation and relapse in an experimental rapid maxillary expansion model

Nigerian journal of clinical practice, 2015-09, Vol.18 (5), p.607-611

2015

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An unusual immune thrombocytopenia case associated with dietary supplements containing 3G (Green tea, Ginseng and Guarana)

Russian open medical journal, 2020-09, Vol.9 (3), p.e0307

2020

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Breastfeeding experience in inborn errors of metabolism other than phenylketonuria

Journal of inherited metabolic disease, 2005-08, Vol.28 (4), p.457-465

2005

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A method to predict effective case depth in ion nitrided steels

Surface & coatings technology, 2005-05, Vol.195 (1), p.116-120

2005

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Asymptomatic adults and older siblings with biotinidase deficiency ascertained by family studies of index cases

Journal of inherited metabolic disease, 2005-12, Vol.28 (6), p.903-912

2005

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Efficacy of light therapy on non-seasonal depression and inflammatory markers

The European journal of psychiatry, 2019-07, Vol.33 (3), p.104-111

2019

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Pharmacokinetics of orally administered tetrahydrobiopterin in patients with phenylalanine hydroxylase deficiency

Journal of inherited metabolic disease, 2006-12, Vol.29 (6), p.725-731

2006

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On Games With Coupled Constraints

IEEE transactions on automatic control, 2015-02, Vol.60 (2), p.358-372

2015

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Silent and symptomatic primary carnitine deficiency within the same family due to identical mutations in the organic cation/carnitine transporter OCTN2

Journal of inherited metabolic disease, 2003-01, Vol.26 (6), p.613-615

2003

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Breast feeding in organic acidaemias

Journal of inherited metabolic disease, 2006-04, Vol.29 (2-3), p.304-310

2006

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Consanguineous 3‐methylcrotonyl‐CoA carboxylase deficiency: Early‐onset necrotizing encephalopathy with lethal outcome

Journal of inherited metabolic disease, 2005-01, Vol.28 (2), p.229-233

2005

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Effect of ion nitriding on fatigue behaviour of AISI 4140 steel

Materials science & engineering. A, Structural materials : properties, microstructure and processing, 2000-02, Vol.279 (1), p.207-216

2000

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Management of phenylketonuria in Europe: Survey results from 19 countries

Molecular genetics and metabolism, 2010-02, Vol.99 (2), p.109-115

2010

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Validity and Reliability Study of the Turkish Version of the Orbach Mikulincer Mental Pain Scale-8 in a Clinical Population

Neuropsychiatric disease and treatment, 2024-01, Vol.20, p.429-438

2024

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Hyperhydroxyprolinaemia detected in newborn screening with tandem mass spectrometry

Journal of inherited metabolic disease, 2004-01, Vol.27 (6), p.781-782

2004

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Stream control in networks with interfering MIMO links

2003 IEEE Wireless Communications and Networking, 2003. WCNC 2003, 2003, Vol.1, p.343-348 vol.1

2003

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Associations Between the Suicidal Ideation and the Tolerance for Psychological Pain and Tolerance for Physical Pain in Patients Diagnosed with Major Depressive Disorder

Neuropsychiatric disease and treatment, 2023-10, Vol.19, p.2283-2294

2023

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Hyperchylomicronaemia due to lipoprotein lipase deficiency as a cause of false‐positive newborn screening for biotinidase deficiency

Journal of inherited metabolic disease, 2005-01, Vol.28 (2), p.137-140

2005

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Seventeen novel mutations that cause profound biotinidase deficiency

Molecular genetics and metabolism, 2002-09, Vol.77 (1), p.108-111

2002

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Incidence of biotinidase deficiency in Turkish newborns

Acta pædiatrica (Oslo), 1998-10, Vol.87 (10), p.1102-1102

1998

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Equilibrium Efficiency Improvement in MIMO Interference Systems: A Decentralized Stream Control Approach

Evaluation of the angulation of the nasal septum deviation as an anatomical variation for increased frequency of antral pseudocyst: a cone-beam computed tomography study

Combined antihypertensive treatment is better than mono-therapy in hypertensive patients

Follow up of phenylketonuria patients

A novel catalyst for diesel soot oxidation

Effects of low-level laser therapy on osteoblastic bone formation and relapse in an experimental rapid maxillary expansion model

An unusual immune thrombocytopenia case associated with dietary supplements containing 3G (Green tea, Ginseng and Guarana)

Breastfeeding experience in inborn errors of metabolism other than phenylketonuria

A method to predict effective case depth in ion nitrided steels

Asymptomatic adults and older siblings with biotinidase deficiency ascertained by family studies of index cases

Efficacy of light therapy on non-seasonal depression and inflammatory markers

Pharmacokinetics of orally administered tetrahydrobiopterin in patients with phenylalanine hydroxylase deficiency

On Games With Coupled Constraints

Silent and symptomatic primary carnitine deficiency within the same family due to identical mutations in the organic cation/carnitine transporter OCTN2

Breast feeding in organic acidaemias

Consanguineous 3‐methylcrotonyl‐CoA carboxylase deficiency: Early‐onset necrotizing encephalopathy with lethal outcome

Effect of ion nitriding on fatigue behaviour of AISI 4140 steel

Management of phenylketonuria in Europe: Survey results from 19 countries

Validity and Reliability Study of the Turkish Version of the Orbach Mikulincer Mental Pain Scale-8 in a Clinical Population

Hyperhydroxyprolinaemia detected in newborn screening with tandem mass spectrometry

Stream control in networks with interfering MIMO links

Associations Between the Suicidal Ideation and the Tolerance for Psychological Pain and Tolerance for Physical Pain in Patients Diagnosed with Major Depressive Disorder

Hyperchylomicronaemia due to lipoprotein lipase deficiency as a cause of false‐positive newborn screening for biotinidase deficiency

Seventeen novel mutations that cause profound biotinidase deficiency

Incidence of biotinidase deficiency in Turkish newborns

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