Continuous glucose monitoring in children with glycogen storage disease type I
Kasapkara, Ç S, Cinasal Demir, G, Hasanoğlu, A, Tümer, L
Published in European journal of clinical nutrition (01.01.2014)
Published in European journal of clinical nutrition (01.01.2014)
Get full text
Journal Article
Home sleep study characteristics in patients with mucopolysaccharidosis
Aslan, A.T, Kasapkara, C, Tumer, L, Kokturk, O
Published in Paediatric respiratory reviews (01.07.2013)
Published in Paediatric respiratory reviews (01.07.2013)
Get full text
Journal Article
P17—Importance of Family Screening in Fabry Disease: Reaching the Bottom of the iceberg
Koca, S, Ezgu, F, Okur, I, Biberoglu, G, Tumer, L, Bakkaloglu, S, Erten, Y, Bahceci, S, Polat, M, Hasanoglu, A
Published in Clinical therapeutics (01.04.2012)
Published in Clinical therapeutics (01.04.2012)
Get full text
Journal Article
O-32 APHERESIS-INDUCIBLE CYTOKINE PATTERN CHANGE IN CHILDREN WITH HOMOZYGOUS FAMILIAL HYPERCHOLESTEROLEMIA
Kucukcongar, A, Yenicesu, I, Tumer, L, Kasapkara, C. Seher, Ezgu, F. Suheyl, Pasaoglu, O, Demirtas, C, Celik, B, Dilsiz, G, Hasanoglu, A
Published in Transfusion and apheresis science (01.09.2012)
Published in Transfusion and apheresis science (01.09.2012)
Get full text
Journal Article
A case of glycogen storage disease type 1a mimicking familial chylomicronemia syndrome
Olgac, A, Okur, İ, Biberoğlu, G, Ezgü, FS, Tümer, L
Published in Balkan journal of medical genetics (27.07.2021)
Published in Balkan journal of medical genetics (27.07.2021)
Get full text
Journal Article
Multisystem involvement in a patient due to accumulation of amylopectin-like material with diminished branching enzyme activity
Eminoglu, T. F., Tumer, L., Okur, I., Olgunturk, R., Hasanoglu, A., Gonul, I. I., Dalgic, B.
Published in Journal of inherited metabolic disease (01.12.2008)
Published in Journal of inherited metabolic disease (01.12.2008)
Get full text
Journal Article
An infantile case of Zellweger syndrome presented with Kabuki-like phenotype
Ezgu, F, Eminoglu, T, Okur, I, Gunduz, M, Tumer, L, Hasanoglu, A, Dalgic, B
Published in Genetic counseling (01.01.2011)
Get full text
Published in Genetic counseling (01.01.2011)
Journal Article
A 7-year-old boy with hand tremors and a novel mutation for L-2-hydroxyglutaric aciduria
Olgac, A, Tekin, Orgun L, Ezgü, FS, Biberoǧlu, G, Tümer, L
Published in Balkan journal of medical genetics (21.12.2019)
Published in Balkan journal of medical genetics (21.12.2019)
Get full text
Journal Article
Bone Mineral Density in Childhood Obesity
Hasanoǧlu, A., Bideci, A., Cinaz, P., Tümer, L., Ünal, S.
Published in Journal of Pediatric Endocrinology and Metabolism (01.03.2000)
Published in Journal of Pediatric Endocrinology and Metabolism (01.03.2000)
Get full text
Journal Article
Effect of enteral and parenteral nutrition on growth parameters of hospitalized Turkish children
Ezgu, F S, Tumer, L, Cinasal, G, Hasanoglu, A, Gunduz, M
Published in Indian pediatrics (01.05.2005)
Get full text
Published in Indian pediatrics (01.05.2005)
Journal Article
Serum Carnitine Levels in Newborns with Perinatal Asphyxia and Relation to Neurologic Prognosis
Ezgü, F.S., Atalay, Y., Hasanoğlu, A., Gücüyener, K., Biberoğlu, G., Koç, E., Ergenekon, E., Tümer, L.
Published in Nutritional neuroscience (01.10.2004)
Published in Nutritional neuroscience (01.10.2004)
Get full text
Journal Article
SRD5A3-CDG: A patient with a novel mutation
Kasapkara, C.S, Tümer, L, Ezgü, F.S, Hasanoğlu, A, Race, V, Matthijs, G, Jaeken, J
Published in European journal of paediatric neurology (01.09.2012)
Published in European journal of paediatric neurology (01.09.2012)
Get full text
Journal Article
Bone Mineral Density and Metabolism in Children Treated with L-Thyroxine
Tümer, L., Hasanoğlu, A., Cinaz, P., Bideci, A.
Published in Journal of Pediatric Endocrinology and Metabolism (01.07.1999)
Published in Journal of Pediatric Endocrinology and Metabolism (01.07.1999)
Get full text
Journal Article
AN EXTREMELY RARE CASE: OSTEOSCLEROTIC METAPHYSEAL DYSPLASIA
KASAPKARA, C. S, KÜCÜKCONGAR, A, BOYUNAGA, O, BEDIR, T, ÖNCÜ, F, HASANOGLU, A, TUMER, L
Published in Genetic counseling (2013)
Get full text
Published in Genetic counseling (2013)
Journal Article
P13—A Case of Fabry Disease With Unexplained Abdominal Pain
Küçükçongar, A, Ezgü, F.S, Tümer, L, Dalgıç, B, Hasanoğlu, A
Published in Clinical therapeutics (01.04.2012)
Published in Clinical therapeutics (01.04.2012)
Get full text
Journal Article
Pattern of human leukocyte antigens in Turkish children with celiac disease
Tümer, Leyla, Altuntaş, Buket, Hasanoğlu, Alev, Söylemezoğlu, Oğuz, Arinsoy, Turgay
Published in Pediatrics international (01.12.2000)
Published in Pediatrics international (01.12.2000)
Get full text
Journal Article
A case with rare type of congenital disorder of glycosylation: PGM1-CDG
Küçükçongar, A, Tümer, L, Ezgü, F Süheyl, Kasapkara, Ç Seher, Jaeken, J, Matthijs, G, Rymen, D, Dalgiç, B, Bıdecı, A, Hasanoğlu, A
Published in Genetic counseling (2015)
Get full text
Published in Genetic counseling (2015)
Journal Article