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Journal of Neurology
|
February 24, 2005
Symptomatic focal mononeuropathies in diabetic patients: increased or not?
Elefterios Stamboulis, Demetris Vassilopoulos, Nikolaos Kalfakis
The Neurologist
|
June 30, 2011
Co-segregation of Huntington disease and hereditary spastic paraplegia in 4 generations
Marios Panas, Georgia Karadima, Nikolaos Kalfakis, et al.
Polish Journal of Pathology : Official Journal of the Polish Society of Pathologists
|
January 15, 2010
Age-related morphometric characteristics of human skeletal muscle in male subjects
Evangelia Kararizou, Panagiota Manta, Nikolaos Kalfakis, et al.
Molecular Genetics and Metabolism
|
November 17, 2007
Low plasma total cholesterol in patients with Huntington's disease and first-degree relatives
Manolis Markianos, Marios Panas, Nikolaos Kalfakis, et al.
Analytical and Quantitative Cytology and Histology
|
March 30, 2005
Morphometric study of the human muscle spindle
Evangelia Kararizou, Panagiota Manta, Nikolaos Kalfakis, et al.
Acta Histochemica
|
September 1, 2007
Spinal muscular atrophy: DNA fragmentation and immaturity of muscle fibers
Demetrios Stathas, Nikolaos Kalfakis, Evangelia Kararizou, et al.
Clinical Rheumatology
|
January 17, 2007
Orofacial dystonia related to Sjogren's syndrome
Sokratis G Papageorgiou, Theodoros Kontaxis, Anastasios Bonakis, et al.
Journal of Neurology
|
November 7, 2002
Friedreich's ataxia mimicking hereditary motor and sensory neuropathy
Marios Panas, Nikolaos Kalfakis, Georgia Karadima, et al.
Acta Histochemica
|
May 30, 2006
Morphological and morphometrical study of human muscle spindles in Werdnig-Hoffmann disease (infantile spinal muscular atrophy type I)
Evangelia Kararizou, Panajota Manta, Nikolaos Kalfakis, et al.
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia
|
June 9, 2009
Asymptomatic elevation of serum creatine kinase leading to the diagnosis of 4q35 facioscapulohumeral muscular dystrophy
Vasiliki Zouvelou, Panagiota Manta, Nikolaos Kalfakis, et al.
Page
of 3
Search research articles
Search
Showing results (1-10 of 24) with videos related to
Sort By:
Page
of 3
Journal of Neurology
|
February 24, 2005
Symptomatic focal mononeuropathies in diabetic patients: increased or not?
Elefterios Stamboulis, Demetris Vassilopoulos, Nikolaos Kalfakis
The Neurologist
|
June 30, 2011
Co-segregation of Huntington disease and hereditary spastic paraplegia in 4 generations
Marios Panas, Georgia Karadima, Nikolaos Kalfakis, et al.
Polish Journal of Pathology : Official Journal of the Polish Society of Pathologists
|
January 15, 2010
Age-related morphometric characteristics of human skeletal muscle in male subjects
Evangelia Kararizou, Panagiota Manta, Nikolaos Kalfakis, et al.
Molecular Genetics and Metabolism
|
November 17, 2007
Low plasma total cholesterol in patients with Huntington's disease and first-degree relatives
Manolis Markianos, Marios Panas, Nikolaos Kalfakis, et al.
Analytical and Quantitative Cytology and Histology
|
March 30, 2005
Morphometric study of the human muscle spindle
Evangelia Kararizou, Panagiota Manta, Nikolaos Kalfakis, et al.
Acta Histochemica
|
September 1, 2007
Spinal muscular atrophy: DNA fragmentation and immaturity of muscle fibers
Demetrios Stathas, Nikolaos Kalfakis, Evangelia Kararizou, et al.
Clinical Rheumatology
|
January 17, 2007
Orofacial dystonia related to Sjogren's syndrome
Sokratis G Papageorgiou, Theodoros Kontaxis, Anastasios Bonakis, et al.
Journal of Neurology
|
November 7, 2002
Friedreich's ataxia mimicking hereditary motor and sensory neuropathy
Marios Panas, Nikolaos Kalfakis, Georgia Karadima, et al.
Acta Histochemica
|
May 30, 2006
Morphological and morphometrical study of human muscle spindles in Werdnig-Hoffmann disease (infantile spinal muscular atrophy type I)
Evangelia Kararizou, Panajota Manta, Nikolaos Kalfakis, et al.
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia
|
June 9, 2009
Asymptomatic elevation of serum creatine kinase leading to the diagnosis of 4q35 facioscapulohumeral muscular dystrophy
Vasiliki Zouvelou, Panagiota Manta, Nikolaos Kalfakis, et al.
Page
of 3