MAHMUT ÇOKER: шукати на сайті Z-Library

European Journal of Pediatrics

Рік:

2001

Мова:

english

Файл:

PDF, 67 KB

english, 2001

Titration of betaine therapy to optimize therapy in an infant with 5,10-methylenetetrahydrofolate reductase deficiency

Sema Kalkan Ucar, Özge Altun Koroğlu, Ömer Berk, Mehmet Yalaz, Nilgün Kültürsay, Henk J. Blom, Mahmut Coker

Журнал:

Рік:

2010

Мова:

english

Файл:

PDF, 79 KB

english, 2010

Alterations of blood pressure in type 1 diabetic children and adolescents

Sukran Darcan, Damla Goksen, Sevgi Mir, Erkin Serdaroglu, Muammer Buyukinan, Mahmut Coker, Afig Berdeli, Timur Köse, Alphan Cura

Журнал:

Pediatric Nephrology

Рік:

2006

Мова:

english

Файл:

PDF, 89 KB

english, 2006

The effect of insulin glargine and nutritional model on metabolic control, quality of life and behavior in children and adolescents with type 1 diabetes mellitus

Damla Goksen, Sukran Darcan, Muammer Buyukinan, Timur Köse, Serpil Erermis, Mahmut Coker

Журнал:

Acta Diabetologica

Рік:

2008

Мова:

english

Файл:

PDF, 178 KB

english, 2008

The first use of N-carbamylglutamate in a patient with decompensated maple syrup urine disease

Sema Kalkan Ucar, Mahmut Coker, Sara Habif, Eylem Ulas Saz, Bulent Karapinar, Hakan Ucar, Omer Kitis, Marinus Duran

Журнал:

Metabolic Brain Disease

Рік:

2009

Мова:

english

Файл:

PDF, 185 KB

english, 2009

Bone mineral density in pediatric and adolescent renal transplant patients: How to evaluate

Damla Gökşen, Şükran Darcan, Pelin Kara, Sevgi Mir, Mahmut Çoker, Caner Kabasakal

Журнал:

Pediatric Transplantation

Рік:

2005

Мова:

english

Файл:

PDF, 119 KB

english, 2005

Permanent neonatal diabetes with arthrogryposis multiplex congenita and neurogenic bladder – a new syndrome?

Damla Goksen, Sukran Darcan, Mahmut Coker, Güzide Aksu, Basak Yıldız, Sinan Kara, Nilgün Kültürsay

Журнал:

Pediatric Diabetes

Рік:

2006

Мова:

english

Файл:

PDF, 71 KB

english, 2006

Combination therapy in treatment of peripheral diabetic neuropathy with severe pain in an adolescent patient

Can Eyigor, Meltem Uyar, Sebnem Pirildar, Mahmut Coker

Журнал:

Pediatric Anesthesia

Рік:

2009

Мова:

english

Файл:

PDF, 50 KB

english, 2009

Low Density Lipoprotein Apheresis in Pediatric Patients With Homozygous Familial Hypercholesterolemia

Mahmut Coker, Sema Kalkan Ucar, Damla Goksen Simsek, Sukran Darcan, Mustafa Bak, Sule Can

Журнал:

Therapeutic Apheresis and Dialysis

Рік:

2009

Мова:

english

Файл:

PDF, 253 KB

english, 2009

Idiopathic Hyperphosphatasia and TNFRSF11B Mutations: Relationships Between Phenotype and Genotype

Belinda Chong, Madhuri Hegde, Matthew Fawkner, Scott Simonet, Hamilton Cassinelli, Mahmut Coker, John Kanis, Joerg Seidel, Cristina Tau, Beyhan Tüysüz, Bilgin Yüksel, Donald Love, Tim Cundy

Журнал:

Journal of Bone and Mineral Research

Рік:

2003

Мова:

english

Файл:

PDF, 846 KB

english, 2003

Clinical overview of children with mucopolysaccharidosis type III A and effect of Risperidone treatment on children and their mothers psychological status

Sema Kalkan Ucar, Burcu Ozbaran, Nagehan Demiral, Zeki Yuncu, Serpil Erermis, Mahmut Coker

Журнал:

Brain and Development

Рік:

2010

Мова:

english

Файл:

PDF, 191 KB

english, 2010

Detection of respiratory syncytial virus in children in the 1993-94 winter season in Izmir, Turkey, by two diagnostic methods

DENIZ DERELI, EKIN ERTEM, DEMIR SERTER, MUSTAFA ŞADIMENT, MAHMUT ÇOKER, REMZIYE TANAÇ

Журнал:

APMIS

Рік:

1994

Мова:

english

Файл:

PDF, 329 KB

english, 1994

Childhood asthma and atmospheric conditions

HASAN YÜKSEL, REMZİYE TANAÇ, ECE TEZ, ESEN DEMIR, MAHMUT ÇOKER

Журнал:

Ali Rıza Alpöz, Mahmut Çoker, Elif Çelen, Nazan Kocatas Ersin, Damla Gökçen, Otto P. van Diggelenc, Jan G.M. Huijmansc

Рік:

1996

Мова:

english

Файл:

PDF, 339 KB

english, 1996

The oral manifestations of Maroteaux-Lamy syndrome (mucopolysaccharidosis VI): A case report

Журнал:

Oral Surgery, Oral Medicine, Oral Pathology, Oral Radiology, and Endodontology

Рік:

2006

Мова:

english

Файл:

PDF, 333 KB

english, 2006

A cross-sectional, mono-centric pilot study of insulin resistance in enzyme replacement therapy patients with Gaucher type I without overweight

Sema Kalkan Ucar, Mahmut Coker, Mehmet Argin, Sezin Akman, Sinan Kara, Damla Goksen Simsek, Sukran Darcan

Журнал:

Hasan Tekgül, Sarenur Tütüncüoglu, Mahmut Çoker, Canan Çoker

Рік:

2009

Мова:

english

Файл:

PDF, 146 KB

english, 2009

Molybdenum cofactor deficiency associated with Dandy–Walker complex

Sertac Arslanoglu, Mehmet Yalaz, Damla Gökşen, Mahmut Çoker, Sarenur Tütüncüoǧlu, Mete Akısu, Şükran Darcan, Nilgun Kultursay, Metin Çiriş, Eren Demirtaş

Журнал:

Brain and Development

Рік:

2001

Мова:

english

Файл:

PDF, 136 KB

english, 2001

Infantile spasm: the effect of corticotropin (ACTH) on the free amino acid profile in cerebrospinal fluid

Журнал:

Brain and Development

Рік:

1999

Мова:

english

Файл:

PDF, 87 KB

english, 1999

Alpha-Galactosidase A Activity Levels in Turkish Male Hemodialysis Patients

Sema Kalkan Uçar, Eser Sozmen, Soner Duman, Ali Başçi, Mahmut Çoker

Журнал:

Therapeutic Apheresis and Dialysis

Рік:

2012

Мова:

english

Файл:

PDF, 311 KB

english, 2012

A patient with WT syndrome and Castleman disease

CANAN VERGIN, NAZAN ÇETINGÜL, KAAN KAVAKLI, SENAY ÖZTOP, FERDA ÖZKINAY, MAHMUT ÇOKER, GÜNGÖR NIŞLI, SALIHA SOYDAN, EROL BALIK, ORHAN AKAR

Журнал:

Рік:

1995

Мова:

english

Файл:

PDF, 525 KB

english, 1995

Diagnostic tools of metabolic and structural brain disturbances in neonatal non-ketotic hyperglycinemia

Demet Terek, Ozge Altun Koroglu, Sezgin Gunes, Mehmet Yalaz, Mete Akisu, Sema Kalkan Uçar, Sarenur Gokben, Mahmut Çoker, Nilgün Kultursay

Журнал:

Journal of Clinical Densitometry

Рік:

2012

Мова:

english

Файл:

PDF, 747 KB

english, 2012

Bone Mineral Density of Healthy Turkish Children and Adolescents

Goksen, Damla, Darcan, Sukran, Coker, Mahmut, Kose, Timur

Журнал:

Рік:

2006

Мова:

english

Файл:

PDF, 229 KB

english, 2006

The missing “link”: an autosomal recessive short stature syndrome caused by a hypofunctional XYLT1 mutation

Schreml, Julia, Durmaz, Burak, Cogulu, Ozgur, Keupp, Katharina, Beleggia, Filippo, Pohl, Esther, Milz, Esther, Coker, Mahmut, Ucar, Sema Kalkan, Nürnberg, Gudrun, Nürnberg, Peter, Kuhn, Joachim, Ozkin

Журнал:

Human Genetics

Рік:

2014

Мова:

english

Файл:

PDF, 718 KB

english, 2014

Molecular analysis in X-linked adrenoleukodystrophy patients: identification of a novel mutation

Durmaz, Asude, Atik, Tahir, Onay, Hüseyin, Canda, Ebru Erbaş, Uçar, Sema Kalkan, Bademkıran, Fikret, Çoker, Mahmut, Çoğulu, Özgür, Özkınay, Ferda

Журнал:

Metabolic Brain Disease

Рік:

2014

Мова:

english

Файл:

PDF, 597 KB

english, 2014

Molecular and clinical delineation of 12 patients with glycogen storage disease type III in Western Turkey

Okubo, Minoru, Ucar, Sema Kalkan, Podskarbi, Teodor, Murase, Toshio, Shin, Yoon S., Coker, Mahmut

Журнал:

Clinica Chimica Acta

Рік:

2015

Мова:

english

Файл:

PDF, 896 KB

english, 2015

Recurrence of carbamoyl phosphate synthetase 1 (CPS1) deficiency in Turkish patients: Characterization of a founder mutation by use of recombinant CPS1 from insect cells expression

Hu, Liyan, Diez-Fernandez, Carmen, Rüfenacht, Véronique, Hismi, Burcu Öztürk, Ünal, Özlem, Soyucen, Erdogan, Çoker, Mahmut, Bayraktar, Bilge Tanyeri, Gunduz, Mehmet, Kiykim, Ertugrul, Olgac, Asburce,

Журнал:

Kologlu, Turan, Ucar, Sema Kalkan, Levent, Erturk, Akcay, Yasemin Delen, Coker, Mahmut, Sozmen, Eser Yıldırım

Рік:

2014

Мова:

english

Файл:

PDF, 1.01 MB

english, 2014

Chitotriosidase as a possible marker of clinically evidenced atherosclerosis in dyslipidemic children

Журнал:

Рік:

2014

Мова:

english

Файл:

PDF, 840 KB

english, 2014

Two novel mutations in acid α-glucosidase gene in two patients with Pompe disease

Aykut, Ayca, Onay, Huseyin, Kose, Melis, Erbas Canda, Ebru, Karaca, Emin, Coker, Mahmut, Ozkinay, Ferda

Журнал:

Рік:

2014

Мова:

english

Файл:

PDF, 891 KB

english, 2014

Analysis of the β-glucocerebrosidase gene in Turkish Gaucher disease patients: mutation profile and description of a novel mutant allele

Karaca, Emin, Kalkan, Sema, Onay, Huseyin, Aykut, Ayca, Coker, Mahmut, Ozkinay, Ferda

Журнал:

Ergun, Pelin, Kagnici, Mehtap, Ucar, Sema Kalkan, Coker, Mahmut, Akcay, Yasemin Delen, Sozmen, Eser Yildirim

Рік:

2012

Мова:

english

Файл:

PDF, 405 KB

english, 2012

Can cathepsin-D and galectin-3 be new inflammation biomarkers in detection of lysosomal diseases?

Журнал:

Şen, Tolga Altuğ, Şimşek, Damla Gökşen, Darcan, Şükran, Çoker, Mahmut

Рік:

2015

Мова:

english

Файл:

PDF, 45 KB

english, 2015

Ghrelin Levels in Children with Constitutional Delay of Growth and Puberty - Original Article

Журнал:

Journal of Clinical Research in Pediatric Endocrinology

Рік:

2010

Мова:

english

Файл:

PDF, 102 KB

english, 2010

Leukocyte cell surface antigens in Gaucher disease: New implications for B-cell proliferation and pathogenesis of myelomatosis

Sozmen, Eser Y., Dondurmaci, Meral, Ucar, Sema Kalkan, Sagin, Ferhan Girgin, Coker, Mahmut

Журнал:

Ucar, Sema Kalkan, Sözmen, Eser, Yıldırım, Hatice Kalkan, Coker, Mahmut

Рік:

2015

Мова:

english

Файл:

PDF, 50 KB

english, 2015

Diagnostic Tools of Early Brain Disturbances in an Asymptomatic Neonate with Maple Syrup Urine Disease

Terek, Demet, Koroglu, Ozge, Yalaz, Mehmet, Gokben, Sarenur, Calli, Cem, Coker, Mahmut, Kultursay, Nilgun

Журнал:

Neuropediatrics

Рік:

2013

Мова:

english

Файл:

PDF, 204 KB

english, 2013

Eyes on MEGDEL: Distinctive Basal Ganglia Involvement in Dystonia Deafness Syndrome

Wortmann, Saskia, van Hasselt, Peter, Barić, Ivo, Burlina, Alberto, Darin, Niklas, Hörster, Friederike, Coker, Mahmut, Kalkan Ucar, Sema, Krumina, Zita, Naess, Karin, Ngu, Lock, Pronicka, Ewa, Riordan

Журнал:

Neuropediatrics

Рік:

2015

Мова:

english

Файл:

PDF, 364 KB

english, 2015

Effect of blueberry tea on lipid and antioxidant status in children with heterozygous familial hypercholesterolemia: pilot study

Журнал:

Clinical Lipidology

Рік:

2014

Мова:

english

Файл:

PDF, 981 KB

english, 2014

Unravelling 5-oxoprolinuria (pyroglutamic aciduria) due to bi-allelic OPLAH mutations: 20 new mutations in 14 families

Sass, Jörn Oliver, Gemperle-Britschgi, Corinne, Tarailo-Graovac, Maja, Patel, Nisha, Walter, Melanie, Jordanova, Albena, Alfadhel, Majid, Barić, Ivo, Çoker, Mahmut, Damli-Huber, Aynur, Faqeih, Eissa A

Журнал:

Orbak, Zerrin, Darcan, Şükran, Çoker, Mahmut, Gökşen, Damla

Рік:

2016

Мова:

english

Файл:

PDF, 297 KB

english, 2016

Maternal and Fetal Serum Insulin-like Growth Factor-I (IGF-I), IGF Binding Protein-3 (IGFBP-3), Leptin Levels and Early Postnatal Growth in Infants Born Asymmetrically Small for Gestational Age

Журнал:

Blood Cells, Molecules, and Diseases

Рік:

2001

Мова:

english

Файл:

PDF, 663 KB

english, 2001

Patients with Gaucher type 1: Switching from imiglucerase to miglustat therapy

Canda, Ebru, Kose, Melis, Kagnici, Mehtap, Ucar, Sema Kalkan, Sozmen, Eser Y., Coker, Mahmut

Журнал:

Рік:

2017

Мова:

english

Файл:

PDF, 543 KB

english, 2017

The Burden Endured by Caregivers of Patients With Morquio A Syndrome

Hendriksz, Christian J., Lavery, Christine, Coker, Mahmut, Ucar, Sema Kalkan, Jain, Mohit, Bell, Lisa, Lampe, Christina

Журнал:

Journal of Inborn Errors of Metabolism & Screening

Рік:

2014

Мова:

english

Файл:

PDF, 599 KB

english, 2014

A novel mutation and in vivo confocal microscopic findings in Fabry disease

Degirmenci, Cumali, Yilmaz, Suzan Guven, Onay, Huseyin, Palamar, Melis, Ucar, Sema Kalkan, Kayikcioglu, Meral, Coker, Mahmut

Журнал:

Saudi Journal of Ophthalmology

Рік:

2017

Мова:

english

Файл:

PDF, 756 KB

english, 2017

False positive diagnosis of lysosomal disease with dried blood spot (DBS) sample; leukocyte number as a challenging factor

Sozmen, Eser Y, Dondurmaci, Meral, Ucar, Sema Kalkan, Coker, Mahmut

Журнал:

Grünert, Sarah Catharina, Schlatter, Sonja Marina, Schmitt, Robert Niklas, Gemperle-Britschgi, Corinne, Mrázová, Lenka, Balcı, Mehmet Cihan, Bischof, Felix, Çoker, Mahmut, Das, Anibh M., Demirkol, Müb

Рік:

2017

Мова:

english

Файл:

PDF, 44 KB

english, 2017

3-Hydroxy-3-methylglutaryl-coenzyme A lyase deficiency: Clinical presentation and outcome in a series of 37 patients

Журнал:

Montaño, Adriana M, Lock-Hock, Ngu, Steiner, Robert D, Graham, Brett H, Szlago, Marina, Greenstein, Robert, Pineda, Mercedes, Gonzalez-Meneses, Antonio, Çoker, Mahmut, Bartholomew, Dennis, Sands, Mark

Рік:

2017

Мова:

english

Файл:

PDF, 757 KB

english, 2017

Clinical course of sly syndrome (mucopolysaccharidosis type VII)

Журнал:

Journal of Medical Genetics

Рік:

2016

Мова:

english

Файл:

PDF, 7.00 MB

english, 2016

A Patient with MSUD: Acute Management with Sodium Phenylacetate/Sodium Benzoate and Sodium Phenylbutyrate

Köse, Melis, Canda, Ebru, Kagnici, Mehtap, Uçar, Sema Kalkan, Çoker, Mahmut

Журнал:

Case Reports in Pediatrics

Рік:

2017

Мова:

english

Файл:

PDF, 1.35 MB

english, 2017

Single center experience of biotinidase deficiency: 259 patients and six novel mutations

Canda, Ebru, Yazici, Havva, Er, Esra, Kose, Melis, Basol, Gunes, Onay, Huseyin, Ucar, Sema Kalkan, Habif, Sara, Ozkinay, Ferda, Coker, Mahmut

Журнал: