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1

A multiple criteria approach for airline passenger satisfaction measurement and service quality improvement

Tsafarakis, Stelios, Kokotas, Theodosios, Pantouvakis, Angelos

Journal:

Journal of Air Transport Management

Year:

2017

Language:

english

File:

PDF, 3.94 MB

english, 2017

2

Drivers, Diversity, and Functions of the Solitary-Bee Microbiota

Voulgari-Kokota, Anna, McFrederick, Quinn S., Steffan-Dewenter, Ingolf, Keller, Alexander

Journal:

Trends in Microbiology

Year:

2019

Language:

english

File:

PDF, 1.15 MB

english, 2019

3

Implementing an mhGAP-based training and supervision package to improve healthcare workersâ competencies and access to mental health care in Malawi

Ahrens, Jen, Kokota, Demoubly, Mafuta, Chitsanzo, Konyani, Mary, Chasweka, Dennis, Mwale, Owen, Stewart, Robert C., Osborn, Madeline, Chikasema, Blessings, Mcheka, Mondie, Blackwood, Douglas, Gilfilla

Journal:

International Journal of Mental Health Systems

Year:

2020

File:

PDF, 984 KB

2020

4

Association of allelic imbalance at locus D13S171 (BRCA2) and p53 alterations with tumor kinetics and chromosomal instability (aneuploidy) in nonsmall cell lung carcinoma

V. G. Gorgoulis, A. Kotsinas, P. Zacharatos, G. Mariatos, T. Liloglou, E. Tsoli, S. Kokotas, C. Fassoulas, J. K. Field, Ch. Kittas

Journal:

Year:

2000

Language:

english

File:

PDF, 567 KB

english, 2000

5

Strong linkage disequilibrium for the frequent GJB2 35delG mutation in the Greek population

Haris Kokotas, Lut Van Laer, Maria Grigoriadou, Vassiliki Iliadou, John Economides, Stella Pomoni, Andreas Pampanos, Nikos Eleftheriades, Elisabeth Ferekidou, Stavros Korres, Aglaia Giannoulia-Karanta

Journal:

American Journal of Medical Genetics Part A

Year:

2008

Language:

english

File:

PDF, 88 KB

english, 2008

6

Complex distal 10q rearrangement in a girl with mild intellectual disability: Follow up of the patient and review of the literature of non-acrocentric satellited chromosomes

Catherine Sarri, Sofia Douzgou, Yolanda Gyftodimou, Zeynep Tümer, Kirstine Ravn, Angela Pasparaki, Theologia Sarafidou, Harry Kontos, Haris Kokotas, Georgia Karadima, Maria Grigoriadou, Effie Pandelia

Journal:

American Journal of Medical Genetics Part A

Year:

2011

Language:

english

File:

PDF, 300 KB

english, 2011

7

Molecular diagnosis of leishmaniosis in dogs: Comparative application of traditional diagnostic methods and the proposed assay on clinical samples

J Ikonomopoulos, S Kokotas, M Gazouli, A Zavras, M Stoitsiou, V.G Gorgoulis

Journal:

Veterinary Parasitology

Year:

2003

Language:

english

File:

PDF, 259 KB

english, 2003

8

Complex chromosome rearrangement in a child with microcephaly, dysmorphic facial features and mosaicism for a terminal deletion del(18)(q21.32-qter) investigated by FISH and array-CGH: Case report

Emmanouil Manolakos, Nadezda Kosyakova, Loreta Thomaidis, Rozita Neroutsou, Anja Weise, Markos Mihalatos, Sandro Orru, Haris Kokotas, George Kitsos, Thomas Liehr, Michael B Petersen

Journal:

Molecular Cytogenetics

Year:

2008

Language:

english

File:

PDF, 1.11 MB

english, 2008

9

Combined 22q11.1-q11.21 deletion with 15q11.2-q13.3 duplication identified by array-CGH in a 6 years old boy

Emmanouil Manolakos, Catherine Sarri, Annalisa Vetro, Konstantinos Kefalas, Eleni Leze, Christalena Sofocleus, George Kitsos, Konstantina Merou, Haris Kokotas, Anna Papadopoulou, Achilleas Attilakos,

Journal:

Molecular Cytogenetics

Year:

2011

Language:

english

File:

PDF, 162 KB

english, 2011

10

Prenatal diagnosis of glycogen storage disease type IV

H. Orhan Akman, Charalampos Karadimas, Yolanda Gyftodimou, Maria Grigoriadou, Haris Kokotas, Anastasia Konstantinidou, Hector Anninos, Efstratios Patsouris, Harshwardhan M. Thaker, Jeffrey B. Kaplan,

Journal:

Prenatal Diagnosis

Year:

2006

Language:

english

File:

PDF, 260 KB

english, 2006

11

Pathologic, radiographic and molecular findings in three fetuses diagnosed with HEM/Greenberg skeletal dysplasia

Anastasia Konstantinidou, Charalampos Karadimas, Hans R. Waterham, Andrea Superti-Furga, Petros Kaminopetros, Maria Grigoriadou, Haris Kokotas, George Agrogiannis, Aglaia Giannoulia-Karantana, Efstrat

Journal:

Prenatal Diagnosis

Year:

2008

Language:

english

File:

PDF, 340 KB

english, 2008

12

Congenital abnormalities of the urachus

I. Kontogeorgos, N. Kokotas

Journal:

International Urology and Nephrology

Year:

1977

Language:

english

File:

PDF, 203 KB

english, 1977

13

Intrinsic endometriosis of the ureter

N. Kokotas, L. Kontogeorgos, E. Kalis, P. Fokitis

Journal:

International Urology and Nephrology

Year:

1981

Language:

english

File:

PDF, 731 KB

english, 1981

14

An unusual case of rectourethral fistula restoration by using a flap from the bladder

N. Kokotas, L. Kontogeorgos

Journal:

International Urology and Nephrology

Year:

1983

Language:

english

File:

PDF, 436 KB

english, 1983

15

Congenital arteriovenous renal fistula

N. Kokotas, N. Xiromeritis, L. Kontogeorgos

Journal:

International Urology and Nephrology

Year:

1982

Language:

english

File:

PDF, 441 KB

english, 1982

16

Benign polyps of the ureter

N. S. Kokotas, J. M. Zissis, J. B. Kastriotis, M. E. Papacharalambous

Journal:

International Urology and Nephrology

Year:

1979

Language:

english

File:

PDF, 1.01 MB

english, 1979

17

Post-cesarean vesicouterine fistula

E. G. Kalis, N. S. Kokotas

Journal:

International Urology and Nephrology

Year:

1980

Language:

english

File:

PDF, 673 KB

english, 1980

18

Multiple enhancers located in a 1-Mb region upstream ofPOU3F4promote expression during inner ear development and may be required for hearing

Silvia Naranjo, Krysta Voesenek, Elisa de la Calle-Mustienes, Alex Robert-Moreno, Haris Kokotas, Maria Grigoriadou, John Economides, Guy Van Camp, Nele Hilgert, Felipe Moreno, Berta Alsina, Michael B.

Journal:

Year:

2010

Language:

english

File:

PDF, 701 KB

english, 2010

19

Mitochondrial deafness

H Kokotas, MB Petersen, PJ Willems

Journal:

Clinical Genetics

Year:

2007

Language:

english

File:

PDF, 192 KB

english, 2007

20

Clinical and molecular aspects of aniridia

H Kokotas, MB Petersen

Journal:

Clinical Genetics

Year:

2010

Language:

english

File:

PDF, 603 KB

english, 2010

21

High frequency of the TARDBP p.Ala382Thr mutation in Sardinian patients with amyotrophic lateral sclerosis

S Orrù, E Manolakos, N Orrù, H Kokotas, V Mascia, C Carcassi, MB Petersen

Journal:

Clinical Genetics

Year:

2012

Language:

english

File:

PDF, 586 KB

english, 2012

22

Mesenchymal stem cells protect CNS neurons against glutamate excitotoxicity by inhibiting glutamate receptor expression and function

A. Voulgari-Kokota, R. Fairless, M. Karamita, V. Kyrargyri, V. Tseveleki, M. Evangelidou, B. Delorme, P. Charbord, R. Diem, L. Probert

Journal:

Experimental Neurology

Year:

2012

Language:

english

File:

PDF, 1002 KB

english, 2012

23

Absence of mutations in the functional domains of the human MDM2 oncogene in non-small cell lung carcinomas

George Mariatos, Vassilis G Gorgoulis, Athanassios Kotsinas, Panayotis Zacharatos, Stavros Kokotas, Dracoulis Yannoukakos, Christos Kittas

Journal:

Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis

Year:

2000

Language:

english

File:

PDF, 108 KB

english, 2000

24

Additional characterization of a hexanucleotide polymorphic site in the first intron of human H-ras gene: comparative study of its alterations in non-small cell lung carcinomas and sporadic invasive breast carcinomas

A. Kotsinas, V.G. Gorgoulis, P. Zacharatos, G. Mariatos, S. Kokotas, T. Liloglou, J. Ikonomopoulos, V. Zoumpourlis, A. Kyroudi, J.K. Field, P.J. Asimacopoulos, C. Kittas

Journal:

Cancer Genetics and Cytogenetics

Year:

2001

Language:

english

File:

PDF, 391 KB

english, 2001

25

Calcification of the Tunica Vaginalis

N. KOKOTAS, L. KONTOGEORGOS, A. KYRIAKIDIS

Journal:

BJU International

Year:

1983

Language:

english

File:

PDF, 82 KB

english, 1983

26

The A1555G mitochondrial DNA mutation in Greek patients with non-syndromic, sensorineural hearing loss

Haris Kokotas, Maria Grigoriadou, George S. Korres, Elisabeth Ferekidou, Eleftheria Papadopoulou, Polyxene Neou, Aglaia Giannoulia-Karantana, Dimitrios Kandiloros, Stavros Korres, Michael B. Petersen

Journal:

Biochemical and Biophysical Research Communications

Year:

2009

Language:

english

File:

PDF, 142 KB

english, 2009

27

Cocirculation of genotypes D4 and D6 in Greece during the 2005 to 2006 measles epidemic

Stavros N. Kokotas, Eugenia Bolanaki, Dionyssios Sgouras, Vasiliki Pogka, Maria Logotheti, Athanasios Kossivakis, Elina Horefti, Kostantinos Papadakos, Andreas Mentis

Journal:

Diagnostic Microbiology and Infectious Disease

Year:

2008

Language:

english

File:

PDF, 551 KB

english, 2008

28

Sudden hearing loss in a family with GJB2 related progressive deafness

Haris Kokotas, Maria Theodosiou, George Korres, Maria Grigoriadou, Elisabeth Ferekidou, Aglaia Giannoulia-Karantana, Michael B. Petersen, Stavros Korres

Journal:

International Journal of Pediatric Otorhinolaryngology

Year:

2008

Language:

english

File:

PDF, 723 KB

english, 2008

29

Homoplasmy of the G7444A mtDNA and heterozygosity of the GJB2 c.35delG mutations in a family with hearing loss

Haris Kokotas, Maria Grigoriadou, Li Yang, Marianne Lodahl, Nanna Dahl Rendtorff, Yolanda Gyftodimou, George S. Korres, Elisabeth Ferekidou, Dimitrios Kandiloros, Stavros Korres, Lisbeth Tranebjærg, M

Journal:

International Journal of Pediatric Otorhinolaryngology

Year:

2011

Language:

english

File:

PDF, 186 KB

english, 2011

30

Compound heterozygosity of the novel c.292C > T (p.R98W) and the c.35delG GJB2 mutations in postlingual, non-syndromic, sensorineural deafness

Michael B. Petersen, Maria Grigoriadou, John Economides, Haris Kokotas

Journal:

International Journal of Pediatric Otorhinolaryngology

Year:

2012

Language:

english

File:

PDF, 540 KB

english, 2012

31

The novel c.247_249delTTC (p.F83del) GJB2 mutation in a family with prelingual sensorineural deafness

Michael B. Petersen, Maria Grigoriadou, Maria Koutroumpe, Haris Kokotas

Journal:

International Journal of Pediatric Otorhinolaryngology

Year:

2012

Language:

english

File:

PDF, 279 KB

english, 2012

32

Screening of a Greek deafness population for the A7445G mitochondrial DNA mutation

Haris Kokotas, Maria Grigoriadou, George S. Korres, Elisabeth Ferekidou, Dimitrios Kandiloros, Stavros Korres, Michael B. Petersen

Journal:

Molecular Genetics and Metabolism

Year:

2010

Language:

english

File:

PDF, 113 KB

english, 2010

33

P53 possibly upregulates the expression of CD58 (LFA-3) and CD59 (MIRL)

F. Sampaziotis, S. Kokotas, V.G. Gorgoulis

Journal:

Medical Hypotheses

Year:

2002

Language:

english

File:

PDF, 257 KB

english, 2002

34

Allelic imbalance at the 5q14 locus is associated with decreased apoptotic rate in non-small cell lung carcinomas (NSCLCs). Possible synergistic effect with p53 gene alterations on apoptosis

Gorgoulis, V.G, Mariatos, G, Manolis, E.N, Zacharatos, P, Kotsinas, A, Liloglou, T, Vogiatzi, T, Tsagkaraki, A, Kokotas, S, Tsoli, E, Alchanatis, M, Sfikakis, P.P, Asimacopoulos, P.J, Field, J.K, Kitt

Journal:

Year:

2000

Language:

english

File:

PDF, 335 KB

english, 2000

35

832 Immunohistochemical analysis of P27KIP1 in superficial transitional cell carcinoma of bladder. Relationship with the tumour kinetics and demographic data

A. Margaritopoulou, A. Paskalidis, P. Zacharatos, N. Mangutis, A. Kotsinas, A. Giouris, N. Kokotas, V. Gorgoulis

Journal:

European Urology Supplements

Year:

2004

Language:

english

File:

PDF, 220 KB

english, 2004

36

Primary malignant melanoma of male urethra

Nikitas S. Kokotas, Efthimios G. Kallis, Panagiotis J. Fokitis

Journal:

Year:

1981

Language:

english

File:

PDF, 1.46 MB

english, 1981

37

Attitudes towards mental illness in Malawi: a cross-sectional survey

Jim Crabb, Robert C Stewart, Demoubly Kokota, Neil Masson, Sylvester Chabunya, Rajeev Krishnadas

Journal:

BMC Public Health

Year:

2012

Language:

english

File:

PDF, 164 KB

english, 2012

38

Combined 22q11.1-q11.21 deletion with 15q11.2-q13.3 duplication identified by array-CGH in a 6 years old boy

Emmanouil Manolakos, Catherine Sarri, Annalisa Vetro, Konstantinos Kefalas, Eleni Leze, Christalena Sofocleus, George Kitsos, Konstantina Merou, Haris Kokotas, Anna Papadopoulou, Achilleas Attilakos,

Journal:

Molecular Cytogenetics

Year:

2011

Language:

english

File:

PDF, 765 KB

english, 2011

39

Are GJB2 mutations an aggravating factor in the phenotypic expression of mitochondrial non-syndromic deafness?

Kokotas, Haris, Grigoriadou, Maria, Korres, George S, Ferekidou, Elisabeth, Giannoulia-Karantana, Aglaia, Kandiloros, Dimitrios, Korres, Stavros, Petersen, Michael B

Journal:

Journal of Human Genetics

Year:

2010

Language:

english

File:

PDF, 240 KB

english, 2010

40

Hypothesizing an Ancient Greek Origin of the GJB2 35delG Mutation: Can Science Meet History?

Kokotas, Haris, Grigoriadou, Maria, Villamar, Manuela, Giannoulia-Karantana, Aglaia, del Castillo, Ignacio, Petersen, Michael B.

Journal:

Genetic Testing and Molecular Biomarkers

Year:

2010

Language:

english

File:

PDF, 80 KB

english, 2010

41

Positive and Negative Implications of Tumor Necrosis Factor Neutralization for the Pathogenesis of Multiple Sclerosis

Taoufik, E., Tseveleki, V., Euagelidou, M., Emmanouil, M., Voulgari-Kokota, A., Haralambous, S., Probert, L.

Journal:

Neurodegenerative Diseases

Year:

2008

Language:

english

File:

PDF, 227 KB

english, 2008

42

4511662 Simultaneous assay for T and B lymphocyte populations and subpopulations

Kokotas, S., Giannaki, M., Horefti, E., Sgouras, D., Logothetis, M., Panagiotopoulos, P., Georgakopoulou, T., Kansouzidou, A., Theodoridou, M., Pangalis, A., Mentis, A.

Journal:

Biotechnology Advances

Year:

1985

Language:

english

File:

PDF, 55 KB

english, 1985

43

P1444 Evaluation of a real-time RT-PCR assay for the diagnosis of measles virus infections during a measles outbreak in Greece

Kokotas, S., Giannaki, M., Horefti, E., Sgouras, D., Logothetis, M., Panagiotopoulos, P., Georgakopoulou, T., Kansouzidou, A., Theodoridou, M., Pangalis, A., Mentis, A.

Journal:

International Journal of Antimicrobial Agents

Year:

2007

Language:

english

File:

PDF, 46 KB

english, 2007

44

Bone marrow mesenchymal stem cell-derived secreted factors promote the proliferation of adult subventricular zone-neural stem cells and foster their stemness in vitro under pathogenic conditions

Voulgari-kokota, Androniki, Buffo, Annalisa, De Rosbo, Nicole Kerlero, Uccelli, Antonio

Journal:

Journal of Neuroimmunology

Year:

2014

Language:

english

File:

PDF, 56 KB

english, 2014

45

Easy, Rapid, and Cost-Effective Methods for Identifying Carriers of Recurrent GJB2 Mutations Causing Nonsyndromic Hearing Impairment in the Greek Population

Kokotas, Haris, Grigoriadou, Maria, Hatzaki, Angeliki, Antoniadi, Thalia, Giannoulia-Karantana, Aglaia, Petersen, Michael B.

Journal:

Genetic Testing and Molecular Biomarkers

Year:

2010

Language:

english

File:

PDF, 566 KB

english, 2010

46

Supernumerary marker chromosome 5 diagnosed by M-FISH in a child with congenital heart defect and unusual face

Sarri, C., Gyftodimou, Y., Grigoriadou, M., Pandelia, E., Kalogirou, S., Kokotas, H., Mrasek, K., Weise, A., Petersen, M.B.

Journal:

Cytogenetic and Genome Research

Year:

2006

Language:

english

File:

PDF, 298 KB

english, 2006

47

Age-related macular degeneration: genetic and clinical findings

Kokotas, Haris, Grigoriadou, Maria, Petersen, Michael B.

Journal:

Clinical Chemistry and Laboratory Medicine

Year:

2011

Language:

english

File:

PDF, 352 KB

english, 2011

48

35-Year Follow-Up of a Case of Ring Chromosome 2: Array-CGH Analysis and Literature Review of the Ring Syndrome

Sarri, Catherine, Douzgou, Sofia, Kontos, Haris, Anagnostopoulou, Katherine, T�mer, Zeynep, Grigoriadou, Maria, Petersen, Michael B., Kokotas, Haris, Merou, Konstantina, Pandelia, Efi, Giouroukou, Ele

Journal:

Cytogenetic and Genome Research

Year:

2015

Language:

english

File:

PDF, 282 KB

english, 2015

49

Biomarkers in primary open angle glaucoma

Kokotas, Haris, Kroupis, Christos, Chiras, Dimitrios, Grigoriadou, Maria, Lamnissou, Klea, Petersen, Michael B., Kitsos, George

Journal:

Clinical Chemistry and Laboratory Medicine

Year:

2012

Language:

english

File:

PDF, 555 KB

english, 2012

50

Molecular technology vs clinical practice: a hypothesis in genetics

Journal:

Journal of Human Genetics

Year:

2010

Language:

english

File:

PDF, 97 KB

english, 2010

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