Limit search to available items
Nearby Subjects are:
Result Page   Prev Next
Add Marked to Bag Add All On Page Add Marked to My Lists
Mark   Year Entries
Myocardium -- Diseases -- Treatment. : Heart : cardiomyopathy : heart failure  2014 1
Myocardium -- Diseases -- Treatment -- Technological innovations : Nanomedicine for ischemic cardiomyopathy progress opportunities, and challenges / edited by Morteza Mahmoudi  2020 1
 

Myocardium Infarction -- See Myocardial infarction


  1
 

Myocardium Inflammation -- See Myocarditis


  1
 

Myocardium Metabolism -- See Heart Metabolism


  1
Myocardium -- metabolism.   6
Myocardium -- pathology.   2
Myocardium -- Pathophysiology.   2
Myocardium -- physiology : Mechanosensitivity of the heart / Andre Kamkin, Irina Kiseleva, editors ; forward by Vadim V. Fedorov  2010 1
Myocardium -- Regeneration.   12
 

Myocardium surgery -- See Cardiac Surgical Procedures


Surgery performed on the heart
  1
 

Myocardium transplantation -- See Heart Transplantation


The transference of a heart from one human or animal to another
  1
Myocardium -- Ultrasonic imaging. : Myocardial imaging : tissue doppler and speckle tracking / edited by Thomas H. Marwick, Cheuk-Man Yu, Jing Ping Sun  2007 1
 

Myoclonic Epilepsy and Ragged Red Fibers -- See MERRF Syndrome


A mitochondrial encephalomyopathy characterized clinically by a mixed seizure disorder, myoclonus, progressive ataxia, spasticity, and a mild myopathy. Dysarthria, optic atrophy, growth retardation, deafness, and dementia may also occur. This condition tends to present in childhood and to be transmitted via maternal lineage. Muscle biopsies reveal ragged-red fibers and respiratory chain enzymatic defects. (From Adams et al., Principles of Neurology, 6th ed, p986)
  1
 

Myoclonic Epilepsy Associated with Ragged-Red Fibers -- See MERRF Syndrome


A mitochondrial encephalomyopathy characterized clinically by a mixed seizure disorder, myoclonus, progressive ataxia, spasticity, and a mild myopathy. Dysarthria, optic atrophy, growth retardation, deafness, and dementia may also occur. This condition tends to present in childhood and to be transmitted via maternal lineage. Muscle biopsies reveal ragged-red fibers and respiratory chain enzymatic defects. (From Adams et al., Principles of Neurology, 6th ed, p986)
  1
 

Myoclonic epilepsy, Infantile -- See Infantile spasms


  1
 

Myoclonic Epilepsy with Ragged-Red Fibers -- See MERRF Syndrome


A mitochondrial encephalomyopathy characterized clinically by a mixed seizure disorder, myoclonus, progressive ataxia, spasticity, and a mild myopathy. Dysarthria, optic atrophy, growth retardation, deafness, and dementia may also occur. This condition tends to present in childhood and to be transmitted via maternal lineage. Muscle biopsies reveal ragged-red fibers and respiratory chain enzymatic defects. (From Adams et al., Principles of Neurology, 6th ed, p986)
  1
 

Myoclonic Seizure -- See Seizures


Clinical or subclinical disturbances of cortical function due to a sudden, abnormal, excessive, and disorganized discharge of brain cells. Clinical manifestations include abnormal motor, sensory and psychic phenomena. Recurrent seizures are usually referred to as EPILEPSY or "seizure disorder."
  1
  Myoclonic seizures -- 2 Related Subjects   2
Myoclonus.   2
 

Myoclonus with Epilepsy with Ragged Red Fibers -- See MERRF Syndrome


A mitochondrial encephalomyopathy characterized clinically by a mixed seizure disorder, myoclonus, progressive ataxia, spasticity, and a mild myopathy. Dysarthria, optic atrophy, growth retardation, deafness, and dementia may also occur. This condition tends to present in childhood and to be transmitted via maternal lineage. Muscle biopsies reveal ragged-red fibers and respiratory chain enzymatic defects. (From Adams et al., Principles of Neurology, 6th ed, p986)
  1
 

Myocyte -- See Muscle Cells


Mature contractile cells, commonly known as myocytes, that form one of three kinds of muscle. The three types of muscle cells are skeletal (MUSCLE FIBERS, SKELETAL), cardiac (MYOCYTES, CARDIAC), and smooth (MYOCYTES, SMOOTH MUSCLE). They are derived from embryonic (precursor) muscle cells called MYOBLASTS
  1
 

Myocyte, Cardiac -- See Myocytes, Cardiac


Striated muscle cells found in the heart. They are derived from cardiac myoblasts (MYOBLASTS, CARDIAC)
  1
 

Myocyte, Skeletal -- See Muscle Fibers, Skeletal


Large, multinucleate single cells, either cylindrical or prismatic in shape, that form the basic unit of SKELETAL MUSCLE. They consist of MYOFIBRILS enclosed within and attached to the SARCOLEMMA. They are derived from the fusion of skeletal myoblasts (MYOBLASTS, SKELETAL) into a syncytium, followed by differentiation
  1
 

Myocyte, Smooth Muscle -- See Myocytes, Smooth Muscle


Non-striated, elongated, spindle-shaped cells found lining the digestive tract, uterus, and blood vessels. They are derived from specialized myoblasts (MYOBLASTS, SMOOTH MUSCLE)
  1
  Myocytes -- 2 Related Subjects   2
 

Myocytes, Cardiac -- See Also Myoblasts, Cardiac


Precursor cells destined to differentiate into cardiac myocytes (MYOCYTES, CARDIAC)
  1
Myocytes, Cardiac. : Calcium handling in hiPSC-derived cardiomyocytes / Lee Yee-Ki, Siu Chung-Wah  2012 1
Myocytes, Cardiac -- chemistry. : Chemical biology in regenerative medicine : bridging stem cells and future therapies / edited by Charles C. Hong, Jijun Hao, and Ada S. Ao  2014 1
Myocytes, Cardiac -- cytology. : Thymosin ß4 coated nanofiber scaffolds for the repair of damaged cardiovascular tissue / Arun Kumar  2015 1
Myocytes, Cardiac -- drug effects. : Thymosin ß4 coated nanofiber scaffolds for the repair of damaged cardiovascular tissue / Arun Kumar  2015 1
Myocytes, Cardiac -- physiology. : Cardiac mechanotransduction / [edited by] Matti Weckström, Pasi Tavi  2007 1
 

Myocytes, Skeletal -- See Muscle Fibers, Skeletal


Large, multinucleate single cells, either cylindrical or prismatic in shape, that form the basic unit of SKELETAL MUSCLE. They consist of MYOFIBRILS enclosed within and attached to the SARCOLEMMA. They are derived from the fusion of skeletal myoblasts (MYOBLASTS, SKELETAL) into a syncytium, followed by differentiation
  1
Myocytes, Smooth Muscle. : Calcium signaling in airway smooth muscle cells / Yong-Xiao Wang, editor  2014 1
 

Myōdō, Satomi, 1896-1978 -- See Satomi, Myōdō, 1896-1978


  1
 

Myodocopida -- See Also the narrower term Cypridinidae


  1
 

Myodynamics -- See Muscles



--individual muscles, e.g. Tensor tympani muscle; also subdivision Muscles under individual organs and regions of the body, e.g. Foot--Muscles; and headings beginning with the word Muscle
  1
 

Myodynia -- See Myalgia


  1
 

Myodystrophia fetalis deformans -- See Arthrogryposis


  1
 

Myodystrophica -- See Muscular Dystrophies


A heterogeneous group of inherited MYOPATHIES, characterized by wasting and weakness of the SKELETAL MUSCLE. They are categorized by the sites of MUSCLE WEAKNESS; AGE OF ONSET; and INHERITANCE PATTERNS
  1
 

Myodystrophicas -- See Muscular Dystrophies


A heterogeneous group of inherited MYOPATHIES, characterized by wasting and weakness of the SKELETAL MUSCLE. They are categorized by the sites of MUSCLE WEAKNESS; AGE OF ONSET; and INHERITANCE PATTERNS
  1
 

Myodystrophies -- See Muscular Dystrophies


A heterogeneous group of inherited MYOPATHIES, characterized by wasting and weakness of the SKELETAL MUSCLE. They are categorized by the sites of MUSCLE WEAKNESS; AGE OF ONSET; and INHERITANCE PATTERNS
  1
 

Myodystrophy -- See Muscular Dystrophies


A heterogeneous group of inherited MYOPATHIES, characterized by wasting and weakness of the SKELETAL MUSCLE. They are categorized by the sites of MUSCLE WEAKNESS; AGE OF ONSET; and INHERITANCE PATTERNS
  1
 

Gyomu no ki -- See Myōe Shōnin yume no ki


  1
 

Yume no ki -- See Myōe Shōnin yume no ki


  1
 

Myōe Shōnin, 1173?-1232 -- See Myōe, 1173?-1232


  1
Myoelectric prosthesis. : Neural prostheses for restoration of sensory and motor function / edited by John K. Chapin, Karen A. Moxon  2001 1
 

Myoelectrically controlled prosthesis -- See Myoelectric prosthesis


  1
 

Myoencephalopathy Ragged-Red Fiber Disease -- See MERRF Syndrome


A mitochondrial encephalomyopathy characterized clinically by a mixed seizure disorder, myoclonus, progressive ataxia, spasticity, and a mild myopathy. Dysarthria, optic atrophy, growth retardation, deafness, and dementia may also occur. This condition tends to present in childhood and to be transmitted via maternal lineage. Muscle biopsies reveal ragged-red fibers and respiratory chain enzymatic defects. (From Adams et al., Principles of Neurology, 6th ed, p986)
  1
 

Myofacial Pain -- See Facial Pain


Pain in the facial region including orofacial pain and craniofacial pain. Associated conditions include local inflammatory and neoplastic disorders and neuralgic syndromes involving the trigeminal, facial, and glossopharyngeal nerves. Conditions which feature recurrent or persistent facial pain as the primary manifestation of disease are referred to as FACIAL PAIN SYNDROMES
  1
Add Marked to Bag Add All On Page Add Marked to My Lists
Result Page   Prev Next