| 1 |
Alikasifoglu A, Unsal Y, Gonc EN, Ozon ZA, Kandemir N, Alikasifoglu M: Long-term effect of
conventional phosphate and calcitriol treatment on metabolic recovery and catch-up growth in
children with PHEX mutation. J Pediatr Endocrinol Metab. 2021 Sept 16, DOI: 10.1515/jpem-2021-0387
|
| 2 |
Alikasifoglu A, Celik NB, Ozon ZA, Gonc EN, Kandemir N. Management of prolactinomas in children and
adolescents; which factors define the response to treatment? Pituitary. 2021, Sept 13,
DOI: 10.1007/s11102-021-01184-x
|
| 3 |
Vuralli D, Gonc N, Ozon A, Ekinci S, Dogan HS, Tekgul S, Alikasifoglu A. Feminizing Adrenocortical
Tumors as a Rare Etiology of Iso/Contrasexual Pseudopuberty. J Clin Res Pediatr Endocrinol. 2021 Aug
12, DOI: 10.4274/jcrpe.galenos.2021.2021.0170
|
| 4 |
Ozsezen B, Emiralioglu N, Ozon A, Akin O, Ademhan Tural D, Sunman B, Hejiyeva A, Hızal M,
Alikasifoglu A, Şimşek Kiper PÖ, Boduroglu K, Utine GE, Yalcin E, Dogru D, Kiper N, Ozcelik U. Sleep
disordered breathing in patients with Prader Willi syndrome: Impact of underlying genetic mechanism.
Respir Med. 2021, Aug 8, 187:106567. DOI: 10.1016/j.rmed.2021.106567
|
| 5 |
Ardıçlı B, User IR, Ciftci AO, Akyüz C, Kutluk MT, , Gonc N, Ozon ZA, Alikasifoglu A, Oguz B,
Haliloglu M, Orhan D, Tanyel FC, Karnak I, Ekinci S. Approach to pheochromocytoma and paraganglioma
in children and adolescents. A retrospective clinical study from a tertiary care center. Journal of
Pediatric Urology. 2021, https://doi.org/10.1016/j.jpurol.2021.01.043
|
| 6 |
Vuralli D, Gonc EN, Ozon A, Kandemir N, Alikasifoglu A. Which parameters predict the beneficial
effect
of GnRHa
treatment on height in girls with central precocious puberty? Clinical Endocrinology. 2021.
|
| 7 |
Canoruc Emet D, Ozon A, Alikasifoglu A, Kandemir N, Gonc N. Alpha‐Melanocyte–Stimulating Hormone is
Elevated in
Hypothalamic Obesity Associated with Childhood Craniopharyngioma . Pediatric Obesity. 2021;
29:402-408.
https://doi.org/10.1002/oby.23087
|
| 8 |
Ardıçlı B, Use IR, Ciftci AO, Akyüz C, Kutluk MT, Yalcin B, Gonc N, Ozon ZA, Alikasifoglu A, Oguz B,
Haliloglu M,
Tanyel FC, Karnak I, Ekinci S.Adrenecortical tumours in children: a review of surgical management at
a
tertiary care
center. ANZ Journal of Surgery. 2021
|
| 9 |
Gunbey C, Ozon A, Gonc EN, Alikasifoğlu A, Karahan S, Kandemir N. Basal
serum thyroxine level should guide initial thyroxine replacement döşe in
neonates with congenital hypothyroidism. J Clin Res Pediatr Endocrinol.
2020 December, doi: 10.4274/jcrpe.galenos.2020.2020.0194.
|
| 10 |
Ozon ZA, Alikasifoglu A, Kandemir N, Aydin B, Gonc EN, Karaosmanoglu B,
Celik NB, Eroglu-Ertugrul NG, Taskiran EZ, Haliloglu G, Oguz KK, Kiper
PO, Yalnizoglu D, Utine GE, Alikasifoglu M. Novel insights into diabetes
mellitus due to DNAJC3-defect: Evolution of neurological and endocrine
phenotype in the pediatric age group Pediatr Diabetes. 2020 Aug 1. doi:
10.1111/pedi.13098. Pediatr Diabetes. 2020. PMID: 32738013
|
| 11 |
Celik NB, Gonc N, Ozon A, Alikasifoglu A , Rauch F , Kandemir N
Treatment response to long term antiresorptive therapy in osteogenesis
imperfecta type VI: does genotype matter? J Pediatr Endocrinol Metab.
2020;33 (12):1617-1624. doi: 10.1515/jpem-2020-0260.
|
| 12 |
Iyigun I, Alikasifoglu A, Gonc N, Ozon A, Eryilmaz Polat S, Hizal M,
Kiper N, Ozcelik U. Obstructive sleep apnea in children with
hypothalamic obesity: Evaluation of possible related factors. Pediatric
Pulmonology. 2020; 55 (12): 3532-3540. doi.org/10.1002/ppul.25097
|
| 13 |
Vurallı D, Gönç EN, Özön ZA, Alikaşifoğlu A. Adequacy of basal
luteinizing hormone levels in the diagnosis of central precocious
puberty. Turkish Archives of Pediatrics. 2020;55(2):131-8.
|
| 14 |
Vurallı D, Gonc N, Ozon A, Kandemir N, Alikasifoglu A. Gender-related
differences in etiology of organic central precocious puberty. Turk J
Pediatr. 2020;62 (5): 763-769
|
| 15 |
Vurallı D, Kosukcu C, Taskıran E, Simsek–Kiper PO, Utine GE, Boduroglu
K, Alikasifoglu A, Alikasifoglu M. Hyperinsulinemic Hypoglycemia in a
Patient with Costello Syndrome: An Etiology to Consider in Hypoglycemia.
Molecular Syndromology. 2020;11(4):207-216.
|
| 16 |
Vurallı D, Gonc EN, Alikasifoglu A, Kandemir N, Ozon ZA. Central nervous
system imaging in girls with central precocious puberty: when is
necessary? Arch Endocrinol Metab. 2020; 64(5):591-596.
doi:10.20945/2359-3997000000259.
|
| 17 |
Unal S, Alikasifoglu A, Ozon A, Gonc N, Kandemir N. Effect of long-term
glucocorticoid therapy on bone mineral density of the patients with
congenital adrenal hyperplasia. Turk J Pediatr. 2020;62(3):359-366. doi:
10.24953/turkjped.2020.03.002.
|
| 18 |
Gonc EN, Ozon ZA, Oguz S, Kabacam S, Taskiran EZ, Kiper POS, Utine GE,
Alikasifoglu A, Kandemir N, Boduroglu OK, Alikasifoglu M. Genetic IGF1R
defects: new cases expand the spectrum of clinical features. J
Endocrinol Invest. 2020;43 (12)1739-1748. doi:
10.1007/s40618-020-01264-y.
|
| 19 |
Iscan AT, Ozsin Ozler C, Ileri Keceli T, Guciz Dogan B, Alikasifoglu A,
Uzamis Tekcicek M. Oral health and halitosis among Type 1 diabetic and
healthy children. J Breath Res. 2020; 14 (3). doi:
10.1088/1752-7163/ab8d8b.
|
| 20 |
Alexandra Dumitrescu, Jiao Fu, Manassawee Korwutthikulrangsri, E. Nazli
Gönç, Laura Sillers, Xiao-Hui Liao, Ayfer Alikasifoglu, Nurgün Kandemir,
Maria Belen Menucci, Kenneth D. Burman, Roy E. Weiss. Clinical and
Molecular Analysis in Two Families with Novel Compound Heterozygous SBP2
(SECISBP2) Mutations. The Journal of Clinical Endocrinology &
Metabolism. 2020;105(3):1-6. doi: 10.1210/clinem/dgz169.
|
| 21 |
Vuralli D, Ozon ZA, Gonc EN, Alikasifoglu A, Kandemir N.Long-term
effects of GnRH agonist treatment on body mass index in girls with
idiopathic central precocious puberty. J Pediatr Endocrinol Metabolism.
J Pediatr Endocrinol Metab. 2020 Jan 28;33(1):99-105. doi:
10.1515/jpem-2019-0214
|
| 22 |
Vuralli D, Alikasifoglu A, Iyigun I, Canoruc D, Ozon A, Gonc N, Kandemir
N. Treatment with depot leuprolide acetate in girls with idiopathic
precocious puberty: What is the best parameter to decide the initial
dose? J Clin Res Pediatr Endocrinol. 2020 Mar 19;12(1):37-44. doi:
10.4274/jcrpe.galenos.2019.2019.0060.
|
| 23 |
Simsek-Kiper PO, Taskiran E, Kosukcu C, Arslan UE, Cormier-Daire V, Gonc
N, Ozon A, Alikasifoglu A, Kandemir N, Utine GE, Alanay Y, Alikasifoglu
M, Boduroglu K. Further expanding the mutational spectrum and
investigation of genotype-phenotype correlation in 3M syndrome. Am J Med
Genet A. 2019;179(7):1157-1172. doi: 10.1002/ajmg.a.61154.
|
| 24 |
Eroglu FK, Ozaltın F, Gonc N, Nalcacıoglu H, Ozcakar ZB, Yalnizoglu D,
Gucer S, Orhan D, Eminoglu FT, Gocmen R, Alikasifoglu A, Topaloglu R,
Düzova A. Response to erly coenzyme Q10 supplementation is not sustained
in CoQ10 deficiency caused by CoQ2 mutation. Pediatric Neurology.
2018;88:71-74. Doi 10.1016/j.pediatrneurol.2018.07.008
|
| 25 |
Akgül S, Alikasifoglu A, Özon A, Gönç N, Düzçeker Y, Örs S, Derman O,
Kanbur N. Can having a sibling with type 1 diabetes cause disordered
eating behaviors? J Pediatr Endocrinol Metab. 2018;31(7):711-716. doi:
10.1515/jpem-2017-0533.
|
| 26 |
Gonc EN, Ozon A, Buyukyilmaz G, Alikasifoglu A, Simsek OP, Kandemir N.
Acquired resistance to pamidronate treated effectively with zoledronate
in juvenile Paget's disease. Osteoporos Int. 2018;29:1471-1474. doi:
10.1007/s00198-018-4443-7.
|
| 27 |
Vurallı D, Kandemir N, Clark G, Orhan D, Alikasifoglu A, Gönç N, Ekinci
S, Özön A. A pheochromocytoma case diagnosed as adrenal incidentaloma.
Turk J Pediatr. 2017;59(2):200-206. doi: 10.24953/turkjped.2017.02.015
|
| 28 |
Gonc N, Ozon A, Alikasifoglu A, Kandemir N. Long term follow-up of a
case with proprotein convertase 1/3 deficiency: Transient diabetes
mellitus with intervening diabetic ketoacidosis during growth hormone
therapy. J Clin Res Pediatr Endocrinol. 2017; Jun 7. doi:
10.4274/jcrpe.3986
|
| 29 |
Vurallı D, Gonc EN, Ozon ZA, Alikasifoglu A, Kandemir N. Clinical and
laboratory parameters predicting a requirement fort he reevaluation of
growth hormone status during growth hormone treatment: retesting early
in the course of GH treatment. Growth Horm IGF Res. 2017 Jun;34:31-37.
doi: 10.1016/j.ghir.2017.05.003.
|
| 30 |
Ahmed Khattab, Shozeb Haider, Ameet Kumar, Samarth Dhawan, Dauood Alam,
Raquel Romero, James Burns, Di Li, Jessica Estatico, Simran Rahi, Saleel
Fatima, Ali Alzahrani, Mona Hafez, Noha Musa, Maryam Razzghy Azar,
Najoua Khaloul, Moez Gribaa, Ali Saad, Ilhem Ben Charfeddine, Berenice
Bilharinho de Mendonçah, Alicia Belgoroskyi, Katja Dumicj, Miroslav
Dumic, Javier Aisenberg, Nurgun Kandemir, Ayfer Alikasifoglu, Alev Ozon,
Nazli Gonc, Tina Cheng, Ursula Kuhnle-Krahl, Marco Cappa, Paul-Martin
Holterhus, Munier A. Nour, Daniele Pacaud, Assaf Holtzman, Sun Li, Mone
Zaidi, Tony Yuen, and Maria I. New. Clinical, genetic, and structural
basis of congenital adrenal hyperplasia due to 11β-hydroxylase
deficiency. Proc Natl Acad Sci U S A. 2017; Mar 7;114(10):E1933-E1940.
doi: 10.1073/pnas.
|
| 31 |
Kandemir N, Yilmaz DY, Gonc EN, Ozon A, Alikasifoglu A, Dursun A, Ozgul
RK. Novel and prevalent CYP11B1 gene mutations in Turkish patients with
11- β hydroxylase deficiency. J Steroid Biochem Mol Biol.
2017;165(PtA)57-63. doi.org/10.1016/j.jsbmb.2016.03.006
|
| 32 |
Soyer T, Karnak İ, Tuncel M, Ekinci S, Andıran F, Çiftçi AÖ, Akçören Z,
Orhan D, Alikaşifoğlu A, Özön A, Tanyel FC. Results of intraoperative
gamma probe survey and frozen section in surgical treatment of
parathyroid adenoma in children. Journal of Pediatric Surgery.
2016;51(9):1492-5. doi: 10.1016/j.j pedsurg.2016.04.007
|
| 33 |
Zengin Akkus P, Çetinkaya A, Ayvaz D, Alikasifoglu M, Alikasifoglu A,
Kandemir N, Tezcan I, Utine GE, Boduroglu K. An adult patient with
monosomy 18p, growth hormone deficiency and selective IgA deficiency. J
Genet Syndr Gene Ther 2016;7(2)
http:/dx.doi.org/10.4172/2157-7412.1000287
|
| 34 |
Vuralli D, Gonc EN, Vidaud D, Ozon A, Alikasifoglu A, Kandemir N. Growth
Hormone Deficiency in a Child with Neurofibromatosis-Noonan Syndrome
(NFNS).J Clin Res Pediatr Endocrinol. 2016;8:96-100. doi:
10.4274/jcrpe.2070.
|
| 35 |
Pehlivantürk Kızılkan M, Kanbur N, Akgul S, Alikasifoglu A. An
Adolescent Boy with Anorexia Nervosa and Hashimoto Thyroiditis. J Clin
Res Pediatr Endocrinol. 2016;8:92-95. doi: 10.4274/jcrpe.2297.
|
| 36 |
Sag E, Gonc N, Alikasifoglu A, Kuşkonmaz B, Uckan D, Ozon A, Kandemir N.
Hyperthyroidism after allogeneic hematopoietic stem cell
transplantation: A report of four cases. J Clin Res Pediatr Endocrinol.
2015;7 (4): 349-354.
|
| 37 |
Gonc EN, Ozon A, Alikasifoglu A, Haliloglu M, Ellard S, Shaw-Smith C,
Kandemir N. Variable phenotype of diabetes mellitus in siblings with a
homozygous PTF1A enhancer mutation. Horm Res Paediatr. 2015;
84(3):206-11.
|
| 38 |
Alikasifoglu A, Vurallı D, Hiort O, Gonc EN, Ozon ZA, Kandemir N. Severe
undervirilisation in a 46,XY case due to a novel mutation in HSD17B3
gene. J Clin Res Pediatr Endocrinol. 2015;7 (1): 249-252.
|
| 39 |
Karadag-Oncel E, Gonc N, Altay O, Cengiz AB, Ozon A, Pinar A, Ceyhan M,
Alikasifoglu A, Akyon Y, Kandemir N, Ozsurekci Y, Kara A. Prevalence of
nasal carriage of methicillin-resistant Staphylococcus aureus in
children with diabetes mellitus: Trends between 2005 and 2013. American
Journal of Infection Control. 2015; 43 (9):1015-7.
|
| 40 |
Karadag-Oncel E, Cakir M, Kara A, Gonc N, Cengiz AB, Ozon A, Ciftci E,
Alikasifoglu A, Ceyhan M, Kandemir N. Evaluation of
hypothalamic-pituitary function in children following acute bacterial
meningitis. Pituitary. 2015; 18:1-7
|
| 41 |
Alikasifoglu A, Vuralli D, Gonc E.N, Ozon A, Kandemir N. Changing
Etiological Trends in Male Precocious Puberty: Evaluation of 100 Cases
with Central Precocious Puberty over the Last Decade. Horm Res Pediatr.
2015;83:340-344.
|
| 42 |
Gonc N, Ozon A, Cakir MD, Alikasifoglu A, Kandemir N. Need for
comprehensive hormonal workup in the management of adrenocortical tumors
in children. J Clin Res Pediatr Endocrinol. 2014 Jun 5;6(2):68-73.
|
| 43 |
Ardicli D, Kandemir N, Alikasifoglu A, Ozon A, Gonc N. Clinical
characteristic of type 1 diabetes over a 40 year period in Turkey:
secular trends towards earlier age of onset. J Pediatr Endocrinol Metab.
2014.
|
| 44 |
Erkocoglu M, Ozon ZA, Gocmen R, Alikasifoglu A, Gonc N, Kandemir N.
Carotid intima media thickness in adolescents with increased risk for
atherosclerosis. Turkish Journal of Pediatrics. 2013;55(5):510-518.
|
| 45 |
Işık E, Beck-Peccoz P, Campi I, Ozon A, Alikasifoglu A, Gonc N, Kandemir
N. Thyroid hormone resistance: A novel mutation in thyroid hormone
receptor beta (THRB) gene – case report. Turk J Pediatr.
2013;55(3):322-327.
|
| 46 |
Kandemir N, Vurallı D, Taşkıran E, Gonç N, Ozon A, Alikasifoglu A,
Yılmaz E. Frequency of mutations in PROP-1 gene in Turkish children with
combined pituitary hormone deficiency. Turk J Pediatr.
2012;54(6):570-575.
|
| 47 |
Alikasifoglu A, Hiort O, Gonc N, Demirbilek H, Isık E, Kandemir N.
17beta-hydroxysteroid dehydrogenase type 3 deficiency as a result of a
homozygous 7 base pair deletion in 17betaHSD3 gene. J Pediatr Endocrinol
Metab. 2012;25(5-6):561-563.
|
| 48 |
Demirbilek H, Gonc EN, Ozon A, Alikasifoglu A, Kandemir N. Evaluation of
serum kisspeptin levels in girls in the diagnosis od central precocious
puberty and in the assessment of pubertal suppression. Journal of
Pediatric Endocrinology and Metabolism. 2012;25(3-4):313-316.
|
| 49 |
Demirbilek H, Alikasifoglu A, Gonc EN, Ozon A, Kandemir N. Assessment of
gonadotropin supression in girls with GnRH analogue for central
precocious puberty; validity of single luteinizing hormone measurement
after luprolide acetate injection. Clinical Endocrinology,
2012;76:126-130.
|
| 50 |
Gonc EN, Ozon Z, Alikasifoglu A, Engiz O, Bulum B, Kandemir N. Is serum
basal 17-OH progesteron a reliable parameter to predict nonclassical
congenital adrenal hyperplasia in premature adrenarche? Turk J Pediatr.
2011;53(3):274-80.
|
| 51 |
Gonc N, Engiz O, Neumann HP, Demirbilek H, Ozon A, Alikasifoglu A,
Kandemir N. Two pediatric patients with Von Hippel-Lindau disease type
2b: from patient to screening, from screening to patient. J Pediatr
Endocrinol Metab. 2011;24(1-2):109-12.
|
| 52 |
Gonc EN, Ozon A, Alikasifoglu A, Kandemir N. Pros of priming in the
diagnosis of growth hormone deficiency. J Pediatr Endocr Met. 2011;
24(1-2)9-11.
|
| 53 |
Kandemir N, Demirbilek H, Ozön ZA, Gönç N, Alikaşifoğlu A. GnRH
stimulation test in precocious puberty: single sample is adequate for
diagnosis and dose adjustment. J Clin Res Pediatr Endocrinol. 2011
Mar;3(1):12-7.
|
| 54 |
Topaloglu R, Bilginer Y, Alikasifoglu A, Ozaltın F, Beşbaş N, Ozen S,
Bakkaloglu A. Neuroendocrine system in familial Mediterranean fever.
Turk J Pediatr. 2010;52(6):588-93.
|
| 55 |
Bilginer Y, Topaloglu R, Alikasifoglu A, Kara N, Besbas N, Ozen S,
Bakkaloglu A. Low cortisol levels in active juvenile idiopathic
arthritis. Clin Rheumatol. 2010 Mar;29(3):309-14.
|
| 56 |
Engiz O, Ozon A, Riepe F, Alikasifoglu A, Gonc N, Kandemir N. Growth
hormone deficiency due to traumatic brain injury in a patient with
X-linked congenital adrenal hypoplasia. The Turkish Journal of
Pediatrics. 2010;52:312-316.
|
| 57 |
Alikasifoglu A, Gonc EN, Ozon A, Şen Y, Kandemir N. The relationship
between serum adiponectin, tumor necrosis factor-alpha, leptin levels
and insulin sensitivity in childhood and adolescent obesity: Adiponectin
is a marker of metabolic syndrome. J Clin Res Ped Endocrinology,
2009;1(5):233-239
|
| 58 |
Akgul S, Balcı Y, Unal S, Alikasifoglu A, Gurgey A. Hypertrichosis: the
possible side effect of cyclosporine in an infant with hemophagocytic
lymphohistiocytosis receiving HLH-2004 chemotherapy protocol. Turk J
Hematol. 2009;26(3):154-6.
|
| 59 |
Demirbilek H, Kandemir N, Gonc EN, Ozon A, Alikasifoglu A. Assesment of
thyroid function during the long course of Hashimoto’s thyroiditis in
children and adolescents. Clin Endocrinol (Oxf). 2009 Sep;71(3):451-4
|
| 60 |
Simsek OP, Utine GE, Alikasifoglu A, Alanay Y, Boduroglu K, Kandemir N.
Rare sex chromosome aneuploidies: 49,XXXXY and 48,XXXY syndromes. The
Turkish Journal of Pediatrics. 2009 May-Jun;51(3):294-7.
|
| 61 |
Gonc EN, Kandemir N, Ozon A, Alikasifoglu A. Final heights of boys with
normal growth hormone responses to provocative tests following priming.
J Pediatr Endocrinol Metab. 2008; 21 (10):963-971
|
| 62 |
Andıran N, Alikasifoglu A, Alanay Y, Yordam N. Cyclic Pamidronate
Treatment in Bruck Syndrome. Pediatr Int. 2008 Dec;50(6):836-8.
|
| 63 |
Dagdelen S, Atmaca A, Alikasifoglu A, Erbas T. Pituitary hypoplasia and
growth hormone deficiency in a woman with glycogen storage disease type
Ia: a case report. J Med Case Reports. 2008 Jun 18;2:210.
|
| 64 |
Unal S, Durmaz E, Erkocoglu M, Bayrakci B, Bircan O, Alikasifoglu A,
Cetin M. The rapid correction of hypercalcemia at presentation of acute
lymphoblastic leukemia using high-dose methylprednisolone. Turkish
Journal of Pediatrics. 2008;50:171-175.
|
| 65 |
Andıran N, Alikasifoglu A, Gonç N, Ozon A, Kandemir N, Yordam N. Cyclic
Pamidronate Therapy in Children with Osteogenesis Imperfecta: Results of
the Treatment and the Follow-up After Discontinuation. J Ped. Endocrinol
Metab. 2008 Jan;21(1):63-72.
|
| 66 |
Sen Y, Kandemir N, Alikasifoglu A, Gonc EN, Ozon A. Prevalence and risk
factors of metabolic syndrome in obese children and adolescents: the
role of the severity of obesity. Eur J Pediatr. 2008;167(10): 1183-89.
|
| 67 |
Demirbilek H, Kandemir N, Gonc EN, Ozon A, Alikasifoglu A, Yordam N.
Hashimoto thyroiditis in children and adolescents: a retrospective study
on clinical, epidemiological and laboratory properties of the disease. J
Ped. Endocrinol Metab. 2007;20(11): 1199-1205.
|
| 68 |
Cetinkaya S, Alikasifoglu A. Central diabetes insipidus associated with
Caroli disease. Indian J Pediatr. 2007;74(4):419-420
|
| 69 |
Ozon A, Cetinkaya S, Alikasifoglu A, Gonc EN, Sen Y, Kandemir N.
Inappropriate use of potent topical glucocorticoids in infants. J Ped.
Endocrinol Metab. 2007;20(2):219-225.
|
| 70 |
Andıran N, Alikasifoglu A, Kupeli S, Yetgin S. Use of biphosphonates for
resistant hypercalcemia in children with acute lymhoblastic leukemia:
report of two cases and review of the literature. Turkish Journal of
Pediatrics. 2006;48:248-252.
|
| 71 |
Utine E, Alikasifoglu A, Alikasifoglu M, Tuncbilek E. Central precocious
puberty in a girl with Williams syndrome: The result of treatment with
GnRH analogue. Eur J Med Genet. 2006 Jan-Feb;49(1):79-82.
|
| 72 |
Harmanci A, Kandemir N, Dagdelen S, Gonc N, Buyukasik Y, Alikasifoglu A,
Kirazli S, Ozon A, Gurlek A. Thrombin-activatable fibrinolysis inhibitor
activity and global fibrinolytic capacity in Type 1 diabetes Evidence
for normal fibrinolytic state. J Diabetes Complications.
2006;20(1):40-4.
|
| 73 |
Yordam N, Gonc EN, Kandemir N, Alikasifoglu A, Ozon A. Ten-tear
experience in management of diabetic ketoacidosis and ketosis: 140
episodes at pediatric age. Turkish Journal of Pediatrics. Turk J
Pediatr. 2005 Oct-Dec;47(4):334-8.
|
| 74 |
Alikasifoglu A, Yetgin S, Cetin M, Tuncer M, Gumruk F, Gurgey A and
Yordam N. Bone mineral density and serum bone turnover markers in
survivors of childhood acute lymphoblastic leukemia: Comparison of
mega-dose methylprednisolon and conventional dose prednisolone
treatments. Am J Hematol. 2005; 80 (2): 114-119.
|
| 75 |
Alikasifoglu A, Gonc EN, Yalcin E, Dogru D and Yordam N. Neonatal
hyperparathyroidism due to maternal hypoparathyroidism and vitamin D
deficiency: A cause of multiple bone fractures. Clinical Pediatrics.
2005;44(3):267-270
|
| 76 |
Ozon A, Alikasifoglu A, Yordam N. Influence of iodine supplementation on
serum insulin-like growth factor (IGF-I) and IGF-binding protein-3
(IGF-BP 3) levels in severe iodine deficiency. Turkish Journal of
Pediatrics. 2004;46:303-308.
|
| 77 |
Gonc EN, Yordam N, Ozon A, Alikasifoglu A, Kandemir N. Endocrinological
outcome of different treatment options in children with
craniopharyngioma: a retrospective analysis of 66 cases. Pediatr
Neurosurg. 2004 May-Jun;40(3):112-9.
|
| 78 |
Gonc EN, Ozon A, Alikasifoglu A, Kandemir N. Type 1 Diabetes Mellitus in
a 3 ½ year-old girl with Turner syndrome. J Ped. Endocrinol Metab.
2002;15:1203-1206.
|
| 79 |
Alikasifoglu A, Özön A, Yordam N. Serum insulin-like growth factor-I
(IGF) and IGF-binding protein-3 levels in severe iodine deficiency.
Turkish Journal of Pediatrics. 2002;44:215-218.
|
| 80 |
Nasonkin IO, Alikasifoglu A, Barrette T, Cheng MM, Thomas PM, Nikitin
AG. Cloning, characterization, and embryonic expression analysis of the
Drosophila melanogaster gene encoding insulin/relaxin-like peptide.
Biochem Biophys Res Commun. 2002 Jul 12;295(2):312-8.
|
| 81 |
Alikasifoglu A, Gonc EN, Akcoren Z, Kale G, Ciftci AO, Senocak ME and
Yordam N. Feminizing Sertoli cell tumor associated with Peutz-Jeghers
syndrome. J Ped. Endocrinol Metab. 2002;15:449-452.
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| 82 |
Alikasifoglu A, Kandemir N, Akalan N, Yordam N. Pituitary adenoma
associated with gigantism and hyperprolactinemia. Pediatr Neurosurg
2001;35:325-328.
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| 83 |
Gönç EN, Yordam N, Kandemir N, Alikasifoglu A. Comparison of stimulated
growth hormone levels in primed versus unprimed provocative tests.
Effect of various testosterone doses on growth hormone levels. Hormone
Research. Horm. Res. 2001;56:32-37
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| 84 |
Yordam N, Alikasifoglu A, Kandemir N, Çağlar M, Balcı S. True
hermaphroditism: Clinical features, genetic variants and gonadal
histology. Journal of Pediatric Endocrinology & Metabolism.
2001;14(4):421-427.
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| 85 |
Seyrantepe V, Kale G, Topaloğlu H, Alikasifoglu A, Özgüç M. Common
deletion of mitochondrial DNA in a 5-year-old girl with failure to
thrive, ptosis, ophtalmoplegia and ragged-red fibers. Brain &
Development. 1999;21:413-415.
|
| 86 |
Nasonkin I, Alikasifoglu A, Ambrose C, Cahill P, Cheng M, Sarniak A,
Egan M, Thomas PM. A novel sulfonylurea Receptor family member expressed
in the embryonic Drosophila dorsal vessel and tracheal system. The
Journal of Biological Chemistry. 1999;274 (42):29420-29425.
|
| 87 |
Yordam N, Özön A, Alikasifoglu A, Özgen A, Ceren N, Zafer Y, Şimşek E.
Iodine deficiency in Turkey. Eur J Pediatr. 1999;158(6):501-505.
|
| 88 |
Alikasifoglu A, Yordam N. The metabolic parameters of obese children and
the role of hyperinsulinism on weight loss. Eur J Paediatr.
1999;158(3):269-270.
|
| 89 |
Yordam N, Kandemir N, Alikasifoglu A. The results of long-term growth
hormone replacement therapy in Turkish children with growth hormone
deficiency. Turkish Journal of Pediatrics. 1998;40(1):55-60.
|
| 90 |
Onur O, Çeliker R, Çetin A, Alikasifoglu A, Uğur O, Başgöze O.
Hypophosphatemic rickets with sacroiliitis-like presentation in an
adolescent. Scand J Rheumatol. 1997;26:332-335.
|
| 91 |
Alikaşifoğlu A, Kandemir N, Çağlar M, Kotiloglu E, Yordam N. Prepubertal
gonadoblastoma in a 46,XY female patient with features of Turner
syndrome. Eur J Paediatr. 1996;155: 653 - 655.
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| 92 |
Yordam N, Kandemir N, Alikaşifoğlu A. Growth hormone therapy in Turner’s
syndrome: Results after 1 year. Turkish Journal of Medical Sciences.
1995; 25: 109-111.
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