Prof.Dr. HÜLYA GÖKMEN ÖZEL

Yayın Ağı

SCI, SSCI ve AHCI İndekslerine Giren Dergilerde Yayınlanan Makaleler

Successful management of rhabdomyolysis with triheptanoin in a child with severe long-chain 3-hydroxyacyl-coenzyme A dehydrogenase (LCHAD) deficiency

KAHRAMAN A. B., YILDIZ Y., GÖKMEN ÖZEL H., KADAYIFÇILAR S., SİVRİ S.

Neuromuscular Disorders , cilt.33, sa.4, ss.315-318, 2023 (SCI-Expanded)

Do Thickening Agents Used in Dysphagia Diet Affect Drug Bioavailability?

ILGAZ F., TİMUR S. S., Eylem C. C., NEMUTLU E., EROĞLU ERDEM Ç., EROĞLU H., et al.

EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES , cilt.174, 2022 (SCI-Expanded)

Medical formula requirements of patients with PKU on BH4 treatment: a systematic review and meta-analysis

Singh R. H., Ilgaz F., Marsaux C. F. M., Pinto A., Rohde C., Karabulut E., et al.

MOLECULAR GENETICS AND METABOLISM , cilt.136, 2022 (SCI-Expanded)

Recommendations on phenylketonuria in Turkey

COŞKUN T., ÇOKER M., Mungan N. O., GÖKMEN ÖZEL H., SİVRİ H. S.

TURKISH JOURNAL OF PEDIATRICS , cilt.64, sa.3, ss.413-434, 2022 (SCI-Expanded)

HOW DO BEDTIME SNACK AND NO SNACK OPTIONS AFFECT OVERNIGHT GLYCEMIA IN YOUNG CHILDREN WITH DIABETES: PRELIMINARY CGM RESULTS

Gokce T., Hatun S., Karakusx K., Mutlu G. Y., Muradoglu S., Eviz E., et al.

DIABETES TECHNOLOGY & THERAPEUTICS , cilt.24, 2022 (SCI-Expanded)

Development of a practical dietitian road map for the nutritional management of phenylketonuria (PKU) patients on pegvaliase

Rocha J. C., Bausell H., Belanger-Quintana A., Bernstein L., GÖKMEN ÖZEL H., Jung A., et al.

MOLECULAR GENETICS AND METABOLISM REPORTS , cilt.28, 2021 (SCI-Expanded)

Protein Substitute Requirements of Patients with Phenylketonuria on BH4 Treatment: A Systematic Review and Meta-Analysis

ILGAZ F., Marsaux C., Pinto A., Singh R., Rohde C., KARABULUT E., et al.

NUTRIENTS , cilt.13, sa.3, 2021 (SCI-Expanded)

Effects of a Psychobiotic Supplement on Serum Brain-derived Neurotrophic Factor Levels in Depressive Patients: A Post Hoc Analysis of a Randomized Clinical Trial

Heidarzadeh-Rad N., GÖKMEN ÖZEL H., Kazemi A., Almasi N., Djafarian K.

JOURNAL OF NEUROGASTROENTEROLOGY AND MOTILITY , cilt.26, sa.4, ss.486-495, 2020 (SCI-Expanded)

Does meal-time insulin dosing based on fat-protein counting give positive results in postprandial glycaemic profile after a high protein-fat meal in adolescents with type 1 diabetes: a randomised controlled trial

Kaya N., Ozel H., Kurtoglu S.

JOURNAL OF HUMAN NUTRITION AND DIETETICS , cilt.33, sa.3, ss.396-403, 2020 (SCI-Expanded) Sürdürülebilir Kalkınma

Does food insulin index in the context of mixed meals affect postprandial metabolic responses and appetite in obese adolescents with insulin resistance? A randomised cross-over trial

CAFEROĞLU Z., HATİPOĞLU N., Ozel H.

BRITISH JOURNAL OF NUTRITION , cilt.122, sa.8, ss.942-950, 2019 (SCI-Expanded)

Long-Term Growth in Phenylketonuria: A Systematic Review and Meta-Analysis

ILGAZ F., Pinto A., Gokmen-Ozel H., Rocha J. C., van Dam E., Ahring K., et al.

NUTRIENTS , cilt.11, sa.9, 2019 (SCI-Expanded)

A series of three case reports in patients with phenylketonuria performing regular exercise: first steps in dietary adjustment

Rocha J. C., van Dam E., Ahring K., Almeida M. F., Belanger-Quintana A., Dokoupil K., et al.

JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , cilt.32, sa.6, ss.635-641, 2019 (SCI-Expanded)

Weaning practices in phenylketonuria vary between health professionals in Europe

Pinto A., Adams S., Ahring K., Allen H., Almeida M. F., Garcia-Arenas D., et al.

MOLECULAR GENETICS AND METABOLISM REPORTS , cilt.18, ss.39-44, 2019 (SCI-Expanded)

Early feeding practices in infants with phenylketonuria across Europe

Pinto A., Adams S., Ahring K., Allen H., Almeida M. F., Garcia-Arenas D., et al.

MOLECULAR GENETICS AND METABOLISM REPORTS , cilt.16, ss.82-89, 2018 (SCI-Expanded)

Nutritional status and food intake are related to malnutrition risk and length of stay in hospitalized patients

YALÇIN T., YÜRÜK A. A., TÜRKOĞLU İ., ILGAZ F., AÇIKGÖZ A., AKSAN A., et al.

PROGRESS IN NUTRITION , cilt.20, sa.3, ss.438-446, 2018 (SCI-Expanded) Sürdürülebilir Kalkınma

Population based study of obesity in Turkey: results of the Turkey Nutrition and Health Survey (TNHS)-2010

Pekcan A. G., Samur G., DİKMEN D., KIZIL M., RAKICIOĞLU N., Yildiz E. A., et al.

PROGRESS IN NUTRITION , cilt.19, sa.3, ss.248-256, 2017 (SCI-Expanded) Sürdürülebilir Kalkınma

Protein substitutes for phenylketonuria in Europe: access and nutritional composition

Pena M. J., de Almeida M. F., van Dam E., Ahring K., Belanger-Quintana A., Dokoupil K., et al.

EUROPEAN JOURNAL OF CLINICAL NUTRITION , cilt.70, sa.7, ss.785-789, 2016 (SCI-Expanded)

Weight Management in Phenylketonuria: What Should Be Monitored?

Rocha J. C., van Rijn M., van Dam E., Ahring K., Belanger-Quintana A., Dokoupil K., et al.

ANNALS OF NUTRITION AND METABOLISM , cilt.68, sa.1, ss.60-65, 2016 (SCI-Expanded)

Special low protein foods for phenylketonuria: availability in Europe and an examination of their nutritional profile

Pena M. J., Almeida M. F., van Dam E., Ahring K., Belanger-Quintana A., Dokoupil K., et al.

ORPHANET JOURNAL OF RARE DISEASES , cilt.10, 2015 (SCI-Expanded)

The challenges of managing coexistent disorders with phenylketonuria: 30 cases

MacDonald A., Ahring K., Almeida M. F., Belanger-Quintana A., Blau N., Burlina A., et al.

MOLECULAR GENETICS AND METABOLISM , cilt.116, sa.4, ss.242-251, 2015 (SCI-Expanded)

Sapropterin dihydrochloride treatment in Turkish hyperphenylalaninemic patients under age four

ÖZLEM U., GÖKMEN ÖZEL H., COŞKUN T., ÖZGÜL R. K., YÜCEL YILMAZ D., BURCU H., et al.

Turkish Journal Of Pediatrics , ss.213-218, 2015 (SCI-Expanded)

Practices in prescribing protein substitutes for PKU in Europe: No uniformity of approach

Aguiar A., Ahring K., Almeida M. F., Assoun M., Belanger Quintana A., Bigot S., et al.

MOLECULAR GENETICS AND METABOLISM , cilt.115, sa.1, ss.17-22, 2015 (SCI-Expanded)

Nutritional content of modular feeds: how accurate is feed production?

Evans S., Daly A., Ashmore C., Gokmen-Ozel H., Dileva R., Dumbleton B., et al.

ARCHIVES OF DISEASE IN CHILDHOOD , cilt.98, sa.3, ss.184-188, 2013 (SCI-Expanded)

Use of sapropterin in the management of phenylketonuria: Seven case reports

Ozel H., Lammardo A. M., Motzfeldt K., Robert M., Rocha J. C., van Rijn M., et al.

MOLECULAR GENETICS AND METABOLISM , cilt.108, sa.2, ss.109-111, 2013 (SCI-Expanded)

Main issues in micronutrient supplementation in phenylketonuria

Lammardo A. M., Robert M., Rocha J. C., van Rijn M., Ahring K., Belanger-Quintana A., et al.

MOLECULAR GENETICS AND METABOLISM , cilt.110, 2013 (SCI-Expanded)

DIETARY SODIUM INTAKE AMONG TURKISH ADULTS

Buyuktuncer-Demirel Z., Kizil M., Aksoy B., Rakicioglu N., Samur G., Yildiz E., et al.

ANNALS OF NUTRITION AND METABOLISM , cilt.63, ss.1089-1090, 2013 (SCI-Expanded)

Micronutrient status in phenylketonuria

Robert M., Rocha J. C., van Rijn M., Ahring K., Belanger-Quintana A., MacDonald A., et al.

MOLECULAR GENETICS AND METABOLISM , cilt.110, 2013 (SCI-Expanded)

Dietary practices in glutaric aciduria type 1 over 16 years

Gokmen-Ozel H., MacDonald A., Daly A., Ashmore C., Preece M. A., Hendriksz C., et al.

JOURNAL OF HUMAN NUTRITION AND DIETETICS , cilt.25, sa.6, ss.514-519, 2012 (SCI-Expanded)

DIETARY MANAGEMENT AND GROWTH OF TETRAHYDROBIOPTERIN RESPONSIVE TURKISH PKU PATIENTS

Gokmen-Ozel H., Unal O., Kalkanoglu-Sivri H. S., Koksal G., DURSUN A., Tokatli A., et al.

JOURNAL OF INHERITED METABOLIC DISEASE , cilt.35, 2012 (SCI-Expanded)

THE 48-HOUR TETRAHYDOBIOPTERIN (BH4) LOADING TEST AND LONG-TERM OUTCOME OF PATIENTS WITH BH4 TREATMENT IN TURKISH PHENYLKETONURIA (PKU) PATIENTS

Unal O., Gokmen-Ozel H., Coskun T., Hismi B., Tokatli A., Dursun A., et al.

JOURNAL OF INHERITED METABOLIC DISEASE , cilt.35, 2012 (SCI-Expanded)

LONG TERM GROWTH STATUS OF TURKISH CHILDREN WITH PHENYLKETONURIA: A RETROSPECTIVE STUDY

Gokmen-Ozel H., Gedikli C., Koksal G., Coskun T.

JOURNAL OF INHERITED METABOLIC DISEASE , cilt.35, 2012 (SCI-Expanded)

Diurnal variation of phenylalanine concentrations in tyrosinaemia type 1: should we be concerned?

Daly A., Gokmen-Ozel H., MacDonald A., Preece M. A., Davies P., Chakrapani A., et al.

JOURNAL OF HUMAN NUTRITION AND DIETETICS , cilt.25, sa.2, ss.111-116, 2012 (SCI-Expanded)

Diet in phenylketonuria: A snapshot of special dietary costs and reimbursement systems in 10 international centers

Belanger-Quintana A., Dokoupil K., Gokmen-Ozel H., Lammardo A. M., MacDonald A., Motzfeldt K., et al.

MOLECULAR GENETICS AND METABOLISM , cilt.105, sa.3, ss.390-394, 2012 (SCI-Expanded)

The development of nonweighed pilot methods for estimating phenylalanine exchanges in non-phenylketonuria volunteers

Gokmen-Ozel H., Daly A., Davies P., MacDonald A.

JOURNAL OF HUMAN NUTRITION AND DIETETICS , cilt.25, sa.1, ss.27-32, 2012 (SCI-Expanded)

Optimising growth in phenylketonuria: Current state of the clinical evidence base

Dokoupil K., GÖKMEN ÖZEL H., Lammardo A. M., Motzfeldt K., Robert M., Rocha J. C., et al.

CLINICAL NUTRITION , cilt.31, sa.1, ss.16-21, 2012 (SCI-Expanded)

Adjusting diet with sapropterin in phenylketonuria: what factors should be considered?

MacDonald A., Ahring K., Dokoupil K., GÖKMEN ÖZEL H., Lammardo A. M., Motzfeldt K., et al.

BRITISH JOURNAL OF NUTRITION , cilt.106, sa.2, ss.175-182, 2011 (SCI-Expanded)

Home visits in phenylketonuria: a 12-month longitudinal study

GOKMEN-OZEL H., Buyuktuncer Z., Koksal G., KALKANOGLU-SIVRI H. S., COŞKUN T.

TURKISH JOURNAL OF PEDIATRICS , cilt.53, sa.2, ss.149-153, 2011 (SCI-Expanded)

Blood phenylalanine control in phenylketonuria: a survey of 10 European centres

AHRING K., BELANGER-QUINTANA A., DOKOUPIL K., Gokmen-Ozel H., LAMMARDO A. M., MACDONALD A., et al.

EUROPEAN JOURNAL OF CLINICAL NUTRITION , cilt.65, sa.2, ss.275-278, 2011 (SCI-Expanded)

Does a lower carbohydrate protein substitute impact on blood phenylalanine control, growth and appetite in children with PKU?

Gokmen-Ozel H., Ferguson C., Evans S., Daly A., MacDonald A.

MOLECULAR GENETICS AND METABOLISM , cilt.104, 2011 (SCI-Expanded)

OPTIMISING GROWTH IN PHENYLKETONURIA: CURRENT STATE OF THE CLINICAL EVIDENCE BASE

Dokoupil K., Gokmen-Ozel H., Lammardo A., Motzfeldt K., Robert M., Rocha J., et al.

JOURNAL OF INHERITED METABOLIC DISEASE , cilt.34, 2011 (SCI-Expanded)

SPECIALIST FEED PRODUCTION FOR PATIENTS WITH INHERITED METABOLIC DISORDERS

Evans S., Daly A., Neville C., Gokmen-Ozel H., Chahal S., MacDonald A.

JOURNAL OF INHERITED METABOLIC DISEASE , cilt.34, 2011 (SCI-Expanded)

The reality of dietary compliance in the management of phenylketonuria

MacDonald A., GÖKMEN ÖZEL H., van Rijn M., Burgard P.

JOURNAL OF INHERITED METABOLIC DISEASE , cilt.33, sa.6, ss.665-670, 2010 (SCI-Expanded)

Errors in emergency feeds in inherited metabolic disorders: a randomised controlled trial of three preparation methods

Gokmen-Ozel H., Daly A., Davies P., Chahal S., MacDonald A.

ARCHIVES OF DISEASE IN CHILDHOOD , cilt.95, sa.10, ss.776-780, 2010 (SCI-Expanded)