Kemal Topaloglu, A.: search on Z-Library

The world's largest scientific articles store. 70,000,000+ articles for free.

1

Normosmic idiopathic hypogonadotropic hypogonadism due to a novel homozygous nonsense c.C969A (p.Y323X) mutation in the KISS1R gene in three unrelated families

Demirbilek, Huseyin, Ozbek, M. Nuri, Demir, Korcan, Kotan, L. Damla, Cesur, Yasar, Dogan, Murat, Temiz, Fatih, Mengen, Eda, Gurbuz, Fatih, Yuksel, Bilgin, Topaloglu, A. Kemal

Journal:

Clinical Endocrinology

Year:

2015

Language:

english

File:

PDF, 430 KB

english, 2015

2

Bone calcium changes during diabetic ketoacidosis: A comparison with lactic acidosis due to volume depletion

A. Kemal Topaloglu, Dincer Yildizdas, H. Levent Yilmaz, Neslihan O. Mungan, Bilgin Yuksel, Guler Ozer

Journal:

Year:

2005

Language:

english

File:

PDF, 174 KB

english, 2005

3

The recent genetics of hypogonadotrophic hypogonadism – novel insights and new questions

Robert K. Semple, A. Kemal Topaloglu

Journal:

Clinical Endocrinology

Year:

2010

Language:

english

File:

PDF, 156 KB

english, 2010

4

Chromium levels in healthy and newly diagnosed type 1 diabetic children

Karagun, Barbaros Sahin, Temiz, Fatih, Ozer, Guler, Yuksel, Bilgin, Topaloglu, Ali Kemal, Mungan, Neslihan Onenli, Mazman, Muhsin, Karagun, Gokhan Murat

Journal:

Pediatrics International

Year:

2012

Language:

english

File:

PDF, 108 KB

english, 2012

5

The Novel Mutation p.Trp147Arg of the Steroidogenic Acute Regulatory Protein Causes Classic Lipoid Congenital Adrenal Hyperplasia with Adrenal Insufficiency and 46,XY Disorder of Sex Development

Yüksel, Bilgin, Kulle, Alexandra E., Gürbüz, Fatih, Welzel, Maik, Kotan, Damla, Mengen, Eda, Holterhus, Paul-Martin, Topaloglu, Ali Kemal, Grötzinger, Joachim, Riepe, Felix G.

Journal:

Hormone Research in Paediatrics

Year:

2013

Language:

english

File:

PDF, 293 KB

english, 2013

6

Primary Hyperparathyroidism in an Infant with Three Parathyroid Glands and Pulmonary Calcinosis

Topaloglu, A. Kemal, Yuksel, Bilgin, Tuncer, Recep, Mungan, Neslihan O., Ozer, Guler

Journal:

Journal of Pediatric Endocrinology and Metabolism

Year:

2001

File:

PDF, 261 KB

2001

7

Does claudication affect the development of coronary collaterals?

Özcan Özdemir, Bilal Geyik, ÖzgÜr Tosun, Mustafa Soylu, Ahmet Duran Demir, Ömer Alyan, Serkan Topaloglu, Dursun Aras, Hatice ŞaŞmaz, Kemal Arda, Sule Korkmaz

Journal:

Heart and Vessels

Year:

2004

Language:

english

File:

PDF, 190 KB

english, 2004

8

P450c17 Deficiency: Clinical and Molecular Characterization of Six Patients

Rosa, S., Duff, C., Meyer, M., Lang-Muritano, M., Balercia, G., Boscaro, M., Kemal Topaloglu, A., Mioni, R., Fallo, F., Zuliani, L., Mantero, F., Schoenle, E. J., Biason-Lauber, A.

Journal:

Journal of Clinical Endocrinology & Metabolism

Year:

2007

Language:

english

File:

PDF, 507 KB

english, 2007

9

Novel Growth Hormone Receptor Gene Mutation in a Patient with Laron Syndrome

Arman, Ahmet, Yüksel, Bilgin, Coker, Ajda, Sarioz, Ozlem, Temiz, Fatih, Topaloglu, Ali Kemal

Journal:

Journal of Pediatric Endocrinology and Metabolism

Year:

2010

Language:

english

File:

PDF, 196 KB

english, 2010

10

Sertoli cell only syndrome with ambiguous genitalia

Gurbuz, Fatih, Ceylaner, Serdar, Erdogan, Seyda, Topaloglu, Ali Kemal, Yuksel, Bilgin

Journal:

Journal of Pediatric Endocrinology and Metabolism

Year:

2016

Language:

english

File:

PDF, 1.66 MB

english, 2016

11

Complete Idiopathic Hypogonadotropic Hypogonadism due to Homozygous GNRH1 Mutations in the Mutational Hot Spots in the Region Encoding the Decapeptide

Mengen, Eda, Tunc, Selma, Kotan, L. Damla, Nalbantoglu, Ozlem, Demir, Korcan, Gurbuz, Fatih, Turan, Ihsan, Seker, Gül, Yuksel, Bilgin, Topaloglu, A. Kemal

Journal:

Hormone Research in Paediatrics

Year:

2016

Language:

english

File:

PDF, 565 KB

english, 2016

12

Inactivating KISS1 Mutation and Hypogonadotropic Hypogonadism

Topaloglu, A. Kemal, Tello, Javier A., Kotan, L. Damla, Ozbek, Mehmet N., Yilmaz, M. Bertan, Erdogan, Seref, Gurbuz, Fatih, Temiz, Fatih, Millar, Robert P., Yuksel, Bilgin

Journal:

Boston Medical and Surgical Journal

Year:

2012

Language:

english

File:

PDF, 698 KB

english, 2012

13

Loss-of-Function Mutations in PNPLA6 Encoding Neuropathy Target Esterase Underlie Pubertal Failure and Neurological Deficits in Gordon Holmes Syndrome

Topaloglu, A. Kemal, Lomniczi, Alejandro, Kretzschmar, Doris, Dissen, Gregory A., Kotan, L. Damla, McArdle, Craig A., Koc, A. Filiz, Hamel, Ben C., Guclu, Metin, Papatya, Esra D., Eren, Erdal, Mengen,

Journal:

Journal of Clinical Endocrinology & Metabolism

Year:

2014

Language:

english

File:

PDF, 1.66 MB

english, 2014

14

[IEEE 2019 Medical Technologies Congress (TIPTEKNO) - Izmir, Turkey (2019.10.3-2019.10.5)] 2019 Medical Technologies Congress (TIPTEKNO) - Effect of Potassium Iodide Use on Anti-Cancer PDT Applications on PC-3 Prostate Cancer Cells

Yunlu, Merve, Ruhi, Mustafa Kemal, Onak, Gunnur, Topaloglu, Nermin

Year:

2019

Language:

english

File:

PDF, 2.31 MB

english, 2019

15

Influence of Metabolic Control on Growth in Homocystinuria due to Cystathionine B-Synthase Deficiency

Topaloglu, Ali Kemal, Sansaricq, Claude, Snyderman, Selma E

Journal:

Pediatric Research

Year:

2001

Language:

english

File:

PDF, 23 KB

english, 2001

16

Prevalence and Associated Phenotypes of PLXNA1 Variants in Normosmic and Anosmic Idiopathic Hypogonadotropic Hypogonadism

Kotan, Leman Damla, Isik, Emregul, Turan, Ihsan, Mengen, Eda, Akkus, Gamze, Tastan, Mehmet, Gurbuz, Fatih, Yuksel, Bilgin, Topaloglu, A. Kemal

Journal:

Clinical Genetics

Year:

2018

Language:

english

File:

PDF, 710 KB

english, 2018

17

Denver developmental screening test II for early identification of the infants who will develop major neurological deficit as a sequalea of hypoxic-ischemic encephalopathy

Olgu Hallioglu, Ali Kemal Topaloglu, Aysegul Zenciroglu, Oznur Duzovali, Esat Yilgor, Sezen Saribas

Journal:

Pediatrics International

Year:

2001

Language:

english

File:

PDF, 74 KB

english, 2001

18

Mitigation and treatment of pollutants from railway and highway runoff by pocket wetland system; A case study

Senduran, Cem, Gunes, Kemal, Topaloglu, Duygu, Dede, Omer Hulusi, Masi, Fabio, Kucukosmanoglu, Ozen Arli

Journal:

Year:

2018

Language:

english

File:

PDF, 1.14 MB

english, 2018

19

Etiological Evaluation of Patients Presenting with Isolated Micropenis to an Academic Health Care Center

Aslan, Tugba Bilmez, Gurbuz, Fatih, Temiz, Fatih, Yuksel, Bilgin, Topaloglu, Ali Kemal

Journal:

Indian Journal of Pediatrics

Year:

2014

Language:

english

File:

PDF, 165 KB

english, 2014

20

TAC3 and TACR3 mutations in familial hypogonadotropic hypogonadism reveal a key role for Neurokinin B in the central control of reproduction

Topaloglu, A Kemal, Reimann, Frank, Guclu, Metin, Yalin, Ayse Serap, Kotan, L Damla, Porter, Keith M, Serin, Ayse, Mungan, Neslihan O, Cook, Joshua R, Ozbek, Mehmet N

Journal:

Nature Genetics

Year:

2008

Language:

english

File:

PDF, 1.10 MB

english, 2008

21

Molecular Genetic Studies in a Case Series of Isolated Hypoaldosteronism due to Biosynthesis Defects or Aldosterone Resistance

Turan, Ihsan, Kotan, L Damla, Tastan, Mehmet, Gurbuz, Fatih, Topaloglu, A Kemal, Yuksel, Bilgin

Journal:

Clinical Endocrinology

Year:

2018

Language:

english

File:

PDF, 576 KB

english, 2018

22

Neurokinin B signalling in the human reproductive axis

A. Kemal Topaloglu, Robert K. Semple

Journal:

Molecular and Cellular Endocrinology

Year:

2011

Language:

english

File:

PDF, 457 KB

english, 2011

23

Wolcott-Rallison Syndrome with Novel EIF2AK3 Gene Mutation

Gürbüz, Fatih, Yüksel, Bilgin, Topaloğlu, Ali Kemal

Journal:

Journal of Clinical Research in Pediatric Endocrinology

Year:

2016

Language:

english

File:

PDF, 260 KB

english, 2016

24

Neurokinin B signaling in puberty: Human and animal studies

A. Kemal Topaloglu

Journal:

Molecular and Cellular Endocrinology

Year:

2010

Language:

english

File:

PDF, 219 KB

english, 2010

25

Molecular analysis ofPROP1,POU1F1,LHX3, andHESX1in Turkish patients with combined pituitary hormone deficiency: a multicenter study

Baş, Firdevs, Uyguner, Z. Oya, Darendeliler, Feyza, Aycan, Zehra, Çetinkaya, Ergun, Berberoğlu, Merih, Şiklar, Zeynep, Öcal, Gönül, Darcan, Şükran, Gökşen, Damla, Topaloğlu, Ali Kemal, Yüksel, Bilgin,

Journal:

Endocrine (Springer)

Year:

2015

Language:

english

File:

PDF, 285 KB

english, 2015

26

The effect of chronic dental inflammation on development of stage 0 medication-related osteonecrosis of the jaw

Topaloglu, Goknur, Koseoglu, Osman Taha, Karaca, Cigdem, Kosemehmetoglu, Kemal

Journal:

Journal of Cranio-Maxillofacial Surgery

Year:

2017

Language:

english

File:

PDF, 5.05 MB

english, 2017

27

A rare variant in human fibroblast activation protein associated with ER stress, loss of enzymatic function and loss of cell surface localisation

Osborne, Brenna, Yao, Tsun-Wen, Wang, Xin Maggie, Chen, Yiqian, Kotan, L. Damla, Nadvi, Naveed A., Herdem, Mustafa, McCaughan, Geoffrey W., Allen, John D., Yu, Denise M.T., Topaloglu, A. Kemal, Gorrel

Journal:

Biochimica et Biophysica Acta (BBA) - Proteins and Proteomics

Year:

2014

Language:

english

File:

PDF, 2.01 MB

english, 2014

28

Three Children with Triple A Syndrome due to a Mutation (R478X) in the AAAS Gene

Yuksel, Bilgin, Braun, Regina, Topaloglu, A. Kemal, Mungan, Neslihan O., Ozer, Guler, Huebner, Angela

Journal:

Hormone Research

Year:

2004

Language:

english

File:

PDF, 104 KB

english, 2004

29

A homozygous recurring mutation in WISP3 causing progressive pseudorheumatoid arthropathy

Temiz, Fatih, Nuri Ozbek, Mehmet, Kotan, Damla, Sangun, Ozlem, Onenli Mungan, Neslihan, Yuksel, Bilgin, Kemal Topaloglu, Ali

Journal:

Journal of Pediatric Endocrinology and Metabolism

Year:

2011

Language:

english

File:

PDF, 366 KB

english, 2011

30

Definition of the phenotypic spectrum of Temtamy preaxial brachydactyly syndrome associated with autosomal recessive CHYS1 mutations

Temtamy, Samia, Aglan, Mona, Topaloglu, A. Kemal, Wollnik, Bernd, Amr, Khalda, El-Badry, Tarek H., Hosny, Gamal A., Eldin, Nermine Salah, Shboul, Mohammad, Herdem, Mustafa, Ong, Junxian, Reversade, Br

Journal:

Middle East Journal of Medical Genetics

Year:

2012

Language:

english

File:

PDF, 681 KB

english, 2012

31

Low Serum Adiponectin Levels in Children and Adolescents with Diabetic Retinopathy

Tasci, Eser, Ozbek, Mehmet Nuri, Onenli Mungan, Neslihan, Temiz, Fatih, Topaloglu, Ali Kemal, Yuksel, Bilgin

Journal:

Eurasian Journal of Medicine

Year:

2011

File:

PDF, 91 KB

2011

32

Chronic mercury intoxication simulating pheochromocytoma: Effect of captopril on urinary mercury excretion

Celalettin Kosan, A Kemal Topaloglu, Behzat Ozkan

Journal:

Pediatrics International

Year:

2001

Language:

english

File:

PDF, 55 KB

english, 2001

33

Update on the Genetics of Idiopathic Hypogonadotropic Hypogonadism

Topaloğlu, A. Kemal

Journal:

Journal of Clinical Research in Pediatric Endocrinology

Year:

2018

Language:

english

File:

PDF, 226 KB

english, 2018

34

Effect of gestational age on plasma fibronectin concentrations in the neonate

A Kemal Topaloglu, Olgu Hallioglu, Oznur Duzovali, Aysel Amac, Esat Yilgor

Journal:

Pediatrics International

Year:

2001

Language:

english

File:

PDF, 105 KB

english, 2001

35

Metabolic acidosis in a patient with type 1 diabetes mellitus complicated by methanol and amitriptyline intoxication

Celik, Umit, Celik, Tamer, Avci, Akkan, Annagur, Ali, Yilmaz, Hayri Levent, Kucukosmanoglu, Osman, Topaloglu, Ali Kemal, Daglioglu, Nebile

Journal:

European Journal of Emergency Medicine

Year:

2009

Language:

english

File:

PDF, 74 KB

english, 2009

36

Extremely immature infant who developed clitoromegaly during the second month of her postnatal life probably due to frequent whole blood transfusion from an adult male

Mustafa Akçam, ALI kemal Topaloglu

Journal:

Pediatrics International

Year:

2003

Language:

english

File:

PDF, 246 KB

english, 2003

37

Wolcott–Rallison syndrome due to the same mutation (W522X) in EIF2AK3 in two unrelated families and review of the literature

M Nuri Ozbek, Valérie Senée, Sehnaz Aydemir, L Damla Kotan, Neslihan O Mungan, Bilgin Yuksel, Cécile Julier, A Kemal Topaloglu

Journal:

Pediatric Diabetes

Year:

2010

Language:

english

File:

PDF, 517 KB

english, 2010

38

Lack of association between plasma leptin levels and appetite in children with iron deficiency

A.Kemal Topaloglu, Olgu Hallioglu, Ali Canim, Oznur Duzovali, Esat Yilgor

Journal:

Year:

2001

Language:

english

File:

PDF, 38 KB

english, 2001

39

Four New Cases of Congenital Secondary Hypothyroidism due to a Splice Site Mutation in the Thyrotropin-β Gene: Phenotypic Variability and Founder Effect

Borck, Guntram, Topaloglu, A. Kemal, Korsch, Eckhard, Martiné, Ursula, Wildhardt, Gabriele, Onenli-Mungan, Neslihan, Yuksel, Bilgin, Aumann, Ulrich, Koch, Gerhard, Ozer, Guler, Pfäffle, Roland, Scherb

Journal:

Journal of Clinical Endocrinology & Metabolism

Year:

2004

Language:

english

File:

PDF, 177 KB

english, 2004

40

Bone Mineral Changes in Acute Metabolic Acidosis due to Acute Gastroenteritis

Dincer Yildizdas, A. Kemal Topaloglu, Neslihan O. Mungan, Bilgin Yuksel, Guler Ozer

Journal:

Calcified Tissue International

Year:

2004

Language:

english

File:

PDF, 69 KB

english, 2004

41

The Authors' Reply: In systemic pseudohypoaldosteronism type 1 skin manifestations are not rare and the disease is not transient

Turan, Ihsan, Topaloglu, Ali Kemal, Yuksel, Bilgin

Journal:

Clinical Endocrinology

Year:

2018

Language:

english

File:

PDF, 394 KB

english, 2018

To build up a library is to create a life. It’s never just a random collection of books.

— Carlos María Domínguez

Official channel

Z-Library Desktop Launcher

Z-Library Since 2009 support@1delivery.pm

EnglishРусскийEspañolItalianoελληνικάاللغة العربيةBahasa IndonesiaBahasa Malaysiaहिन्दीDeutschFrançaisPortuguêsУкраїнськаPolski中文繁體中文日本語Tiếng ViệtAzərbaycan DiliՀայոց լեզուภาษาไทยTürk Diliქართველიবাংলাپښتوతెలుగుاردو한국어SrpskiБългарски