Maria Diakou

University of Ioannina

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Moses Elisaf

Aristotle University of Thessaloniki

George Miltiadous

University of Ioannina

Marios A. Cariolou

Cyprus Institute of Neurology and Genetics

Stavroulla Xenophontos

Cyprus Institute of Neurology and Genetics

Dimitrios I. Fotiadis

University of Ioannina

Anastasia Zikou

University of Ioannina

Sofia Tsouli

University of Ioannina

Athanassios P. Kyritsis

University of Ioannina

Maria I. Argyropoulou

University of Ioannina

Dina Baga

University of Ioannina

Cooperative Institutions

University of Ioannina

University Hospital of Ioannina

National and Kapodistrian University of Athens

Mother Teresa Hospital

Cyprus Institute of Neurology and Genetics

University of Medicine Tirana

Universidad Politécnica de Madrid

University College London

National Institutes of Health

The Royal Free Hospital

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Cerebral venous thrombosis in an adolescent with ulcerative colitis

Brain and Development (2010)

Maria Diakou Vasiliki Kostadima Sotirios Giannopoulos Anastasia Zikou Maria I. Argyropoulou

Pathophysiology

10.1016/j.braindev.2010.04.006

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Citations (22)

Cerebral Venous Thrombosis in a Patient with Sarcoidosis

Internal Medicine (2009)

A. Selvi Maria Diakou Sotirios Giannopoulos Anastasia Zikou Maria I. Argyropoulou

Cerebral venous thrombosis (CVT) may present with a variety of symptoms and findings consisting of either only persistent headache, or slowly progressive stroke over several days, or even coma. CVT may develop in relation to hypercoagulable states. However, even after extensive investigation, a predisposing factor could not be identified in some cases. We report a case of CVT associated with heterozygous V Leiden mutation and sarcoidosis. Since most factor V gene heterozygous individuals do not exhibit clinical thrombotic events, the venous thrombosis of our patient suggests convergence of an inherited predisposition (heterozygous factor V Leiden mutation) with an acquired thrombogenic stimulus (sarcoidosis). Early diagnosis and treatment with anticoagulation is pivotal for a favorable outcome.

Stroke

10.2169/internalmedicine.48.1809

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Citations (18)

Abstract: P834 MUTATIONAL ANALYSIS IN NORTHWESTERN GREECE PATIENTS WITH CLINICAL DIAGNOSIS OF FAMILIAL HYPERCHOLESTEROLEMIA

Atherosclerosis Supplements (2009)

Maria Diakou George Miltiadous Stavroulla Xenophontos Marios A. Cariolou Moses Elisaf

10.1016/s1567-5688(09)71188-2

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Spectrum of LDLR gene mutations, including a novel mutation causing familial hypercholesterolaemia, in North-western Greece

European Journal of Internal Medicine (2011)

Maria Diakou George Miltiadous Stavroulla Xenophontos Panayiotis Manoli Marios A. Cariolou

10.1016/j.ejim.2011.01.003

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Citations (16)

Abstract: P835 CHARACTERIZATION OF THE LOW DENSITY LIPOPROTEIN RECEPTOR (LDLR) GENE MUTATION IN ALBANIA

Atherosclerosis Supplements (2009)

Maria Diakou George Miltiadous Stavroulla Xenophontos Marios A. Cariolou Moses Elisaf

10.1016/s1567-5688(09)71189-4

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FAMILIAL HYPERCHOLESTEROLAEMIA IN NORTHWESTERN GREECE

Atherosclerosis Supplements (2008)

Maria Diakou George Miltiadous Zoi Mitrogianni M. Kalogirou X. Millionis

10.1016/s1567-5688(08)70308-8

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Citations (2)

Using partial decision trees to predict Parkinson’s symptoms: A new approach for diagnosis and therapy in patients suffering from Parkinson’s disease

Computers in Biology and Medicine (2011)

Themis P. Exarchos Alexandros T. Tzallas Dina Baga Dimitra A. Chaloglou Dimitrios I. Fotiadis

Association (psychology)

10.1016/j.compbiomed.2011.11.008

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Citations (33)

PERFORM: A platform for monitoring and management of chronic neurodegenerative diseases: The Parkinson and Amyotrophic Lateral Sclerosis case

Dina Baga Dimitrios I. Fotiadis Spiros Konitsiotis Sofia Tsouli Maria Diakou

In this work we present a system for the monitoring and management of neurodegenerative diseases, such as the Parkinson's Disease (PD) and amyotrophic lateral sclerosis (ALS). The purpose of the system is to monitor patient's motor symptoms, and assist the clinician in the evaluation of both the current patient status and the disease progression. The system progresses one step further and suggests appropriate patient treatment changes, based on previously stored or accumulated medical knowledge. In this work, we focus on the description of the wearable platforms used to monitor the patient motor status at the patient's environment.

Motor symptoms

Disease monitoring

10.1109/ner.2009.5109220

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Citations (9)

Pharmacological treatment of non-alcoholic steatohepatitis: The current evidence

Scandinavian Journal of Gastroenterology (2006)

Maria Diakou Evangelos Liberopoulos Dimitri P. Mikhailidis E.V. Tsianos Andrew K. Burroughs

Non-alcoholic fatty liver disease (NAFLD) is a clinicopathologic term that encompasses two main components: 1) simple steatosis (non-alcoholic fatty liver (NAFL)), a benign condition characterized ...

Steatohepatitis

10.1080/00365520601058395

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Citations (12)

Original research Characterization of low density lipoprotein receptor (LDLR) gene mutations in Albania

Archives of Medical Science (2010)

Maria Diakou George Miltiadous Stavroulla Xenophontos Marios A. Cariolou Nevila Heta

ENWEndNote BIBJabRef, Mendeley RISPapers, Reference Manager, RefWorks, Zotero AMA Diakou M, Miltiadous G, Xenophontos S, et al. Original research Characterization of low density lipoprotein receptor (LDLR) gene mutations in Albania. Archives of Medical Science. 2010;6(2):198-200. doi:10.5114/aoms.2010.13894. APA Diakou, M., Miltiadous, G., Xenophontos, S., Cariolou, M., Heta, N., & Korita, I. et al. (2010). Original research Characterization of low density lipoprotein receptor (LDLR) gene mutations in Albania. Archives of Medical Science, 6(2), 198-200. https://doi.org/10.5114/aoms.2010.13894 Chicago Diakou, Maria, George Miltiadous, Stavroula Xenophontos, Marios Cariolou, Nevila Heta, Irena Korita, and Anyla Bulo et al. 2010. "Original research Characterization of low density lipoprotein receptor (LDLR) gene mutations in Albania". Archives of Medical Science 6 (2): 198-200. doi:10.5114/aoms.2010.13894. Harvard Diakou, M., Miltiadous, G., Xenophontos, S., Cariolou, M., Heta, N., Korita, I., Bulo, A., Refatllari, E., Bairaktari, E., and Elisaf, M. (2010). Original research Characterization of low density lipoprotein receptor (LDLR) gene mutations in Albania. Archives of Medical Science, 6(2), pp.198-200. https://doi.org/10.5114/aoms.2010.13894 MLA Diakou, Maria et al. "Original research Characterization of low density lipoprotein receptor (LDLR) gene mutations in Albania." Archives of Medical Science, vol. 6, no. 2, 2010, pp. 198-200. doi:10.5114/aoms.2010.13894. Vancouver Diakou M, Miltiadous G, Xenophontos S, Cariolou M, Heta N, Korita I et al. Original research Characterization of low density lipoprotein receptor (LDLR) gene mutations in Albania. Archives of Medical Science. 2010;6(2):198-200. doi:10.5114/aoms.2010.13894.

Proband

10.5114/aoms.2010.13894

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Citations (7)