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Mark   Year Entries
Music Austria Biography : Neumayr, Anton.  1994 1
Music Biography   2
Music Psychology   8
Music Psychology Congresses   1991 1
Music Therapy   14
Music Therapy Case Reports   3
Music Therapy Congresses   1993 1
Music Therapy Methods   11
Musical Intervals And Scales : Meisner, Gary.  1990 1
Musicals Excerpts Vocal Scores With Piano : Rodgers, Richard,  1990 1
 

Musk Mg -- See Myasthenia Gravis


A disorder of neuromuscular transmission characterized by fatigable weakness of cranial and skeletal muscles with elevated titers of ACETYLCHOLINE RECEPTORS or muscle-specific receptor tyrosine kinase (MuSK) autoantibodies. Clinical manifestations may include ocular muscle weakness (fluctuating, asymmetric, external ophthalmoplegia; diplopia; ptosis; and weakness of eye closure) and extraocular fatigable weakness of facial, bulbar, respiratory, and proximal limb muscles. The disease may remain limited to the ocular muscles (ocular myasthenia). THYMOMA is commonly associated with this condition.
  1
 

Musk Myasthenia Gravis -- See Myasthenia Gravis


A disorder of neuromuscular transmission characterized by fatigable weakness of cranial and skeletal muscles with elevated titers of ACETYLCHOLINE RECEPTORS or muscle-specific receptor tyrosine kinase (MuSK) autoantibodies. Clinical manifestations may include ocular muscle weakness (fluctuating, asymmetric, external ophthalmoplegia; diplopia; ptosis; and weakness of eye closure) and extraocular fatigable weakness of facial, bulbar, respiratory, and proximal limb muscles. The disease may remain limited to the ocular muscles (ocular myasthenia). THYMOMA is commonly associated with this condition.
  1
 

Muslims -- See Islam


A monotheistic religion promulgated by the Prophet Mohammed with Allah as the deity.
  1
Mustang Juvenile Literature : Featherly, Jay.  1986 1
Mustard Gas Toxicity : Smith, Susan L.,  2017 1
 

Mustela Putorius -- See Ferrets


Semidomesticated variety of European polecat much used for hunting RODENTS and/or RABBITS and as a laboratory animal. It is in the subfamily Mustelinae, family MUSTELIDAE.
  1
 

Mustela Putorius Furo -- See Ferrets


Semidomesticated variety of European polecat much used for hunting RODENTS and/or RABBITS and as a laboratory animal. It is in the subfamily Mustelinae, family MUSTELIDAE.
  1
Mutagenesis : Frickel, Scott.  2004 1
 

Mutagenesis Site Directed -- See Also Gene Editing


Genetic engineering or molecular biology techniques that involve DNA REPAIR mechanisms for incorporating site-specific modifications into a cell's genome.
  1
 

Mutagens -- See Also Mutagenesis


Process of generating a genetic MUTATION. It may occur spontaneously or be induced by MUTAGENS.
  1
Mutagens Adverse Effects : Frickel, Scott.  2004 1
 

Mutation -- See Also Mutagenesis


Process of generating a genetic MUTATION. It may occur spontaneously or be induced by MUTAGENS.
  1
  Mutation Accumulation -- 2 Related Mesh Subjects   2
Mutation Genetics : McConkey, Edwin H.  2004 1
Mutter Museum : Aptowicz, Cristin O'Keefe,  2014 1
Mutter Thomas D Thomas Dent 1811 1859 : Aptowicz, Cristin O'Keefe,  2014 1
Myasthenia Gravis Diagnosis Autobiography : Atkins, ChloĆ« G. K.  2010 1
 

Myasthenic Syndromes Congenital -- See Also Myasthenia Gravis


A disorder of neuromuscular transmission characterized by fatigable weakness of cranial and skeletal muscles with elevated titers of ACETYLCHOLINE RECEPTORS or muscle-specific receptor tyrosine kinase (MuSK) autoantibodies. Clinical manifestations may include ocular muscle weakness (fluctuating, asymmetric, external ophthalmoplegia; diplopia; ptosis; and weakness of eye closure) and extraocular fatigable weakness of facial, bulbar, respiratory, and proximal limb muscles. The disease may remain limited to the ocular muscles (ocular myasthenia). THYMOMA is commonly associated with this condition.
  1
Mycobacterium Avium Subsp Paratuberculosis   2007 1
 

Mycobacterium Influenzae -- See Haemophilus influenzae


A species of HAEMOPHILUS found on the mucous membranes of humans and a variety of animals. The species is further divided into biotypes I through VIII.
  1
 

Mycobacterium Paratuberculosis -- See Mycobacterium avium subsp. paratuberculosis


A subspecies of gram-positive, aerobic bacteria. It is the etiologic agent of Johne's disease (PARATUBERCULOSIS), a chronic GASTROENTERITIS in RUMINANTS.
  1
Mycology Laboratory Manuals : Larone, Davise Honig,  2011 1
 

Mycorrhizae -- See Also Symbiosis


The relationship between two different species of organisms that are interdependent; each gains benefits from the other or a relationship between different species where both of the organisms in question benefit from the presence of the other.
  1
 

Mycoses -- See Also Antifungal Agents


Substances that destroy fungi by suppressing their ability to grow or reproduce. They differ from FUNGICIDES, INDUSTRIAL because they defend against fungi present in human or animal tissues.
  1
Mycoses   2
Mycoses History : Homei, Aya,  2013 1
 

Mycotic Aneurysm Intracranial -- See Intracranial Aneurysm


Abnormal outpouching in the wall of intracranial blood vessels. Most common are the saccular (berry) aneurysms located at branch points in CIRCLE OF WILLIS at the base of the brain. Vessel rupture results in SUBARACHNOID HEMORRHAGE or INTRACRANIAL HEMORRHAGES. Giant aneurysms (>2.5 cm in diameter) may compress adjacent structures, including the OCULOMOTOR NERVE. (From Adams et al., Principles of Neurology, 6th ed, p841)
  1
 

Mycotoxin -- See Mycotoxins


Toxic compounds produced by FUNGI.
  1
  Mycotoxins -- 2 Related Mesh Subjects   2
Mycotoxins : Christensen, Clyde Martin,  1975 1
Mycotoxins Toxicity : Marasas, W. F. O.  1987 1
 

Myelin Oligodendrocyte Glycoprotein -- See Also Multiple Sclerosis


An autoimmune disorder mainly affecting young adults and characterized by destruction of myelin in the central nervous system. Pathologic findings include multiple sharply demarcated areas of demyelination throughout the white matter of the central nervous system. Clinical manifestations include visual loss, extra-ocular movement disorders, paresthesias, loss of sensation, weakness, dysarthria, spasticity, ataxia, and bladder dysfunction. The usual pattern is one of recurrent attacks followed by partial recovery (see MULTIPLE SCLEROSIS, RELAPSING-REMITTING), but acute fulminating and chronic progressive forms (see MULTIPLE SCLEROSIS, CHRONIC PROGRESSIVE) also occur. (Adams et al., Principles of Neurology, 6th ed, p903)
  1
 

Myelitis Transverse -- See Also Multiple Sclerosis


An autoimmune disorder mainly affecting young adults and characterized by destruction of myelin in the central nervous system. Pathologic findings include multiple sharply demarcated areas of demyelination throughout the white matter of the central nervous system. Clinical manifestations include visual loss, extra-ocular movement disorders, paresthesias, loss of sensation, weakness, dysarthria, spasticity, ataxia, and bladder dysfunction. The usual pattern is one of recurrent attacks followed by partial recovery (see MULTIPLE SCLEROSIS, RELAPSING-REMITTING), but acute fulminating and chronic progressive forms (see MULTIPLE SCLEROSIS, CHRONIC PROGRESSIVE) also occur. (Adams et al., Principles of Neurology, 6th ed, p903)
  1
 

Myelocytic Leukemia -- See Leukemia, Myeloid


Form of leukemia characterized by an uncontrolled proliferation of the myeloid lineage and their precursors (MYELOID PROGENITOR CELLS) in the bone marrow and other sites.
  1
 

Myelocytic Leukemia Chronic -- See Leukemia, Myelogenous, Chronic, BCR-ABL Positive


Clonal hematopoetic disorder caused by an acquired genetic defect in PLURIPOTENT STEM CELLS. It starts in MYELOID CELLS of the bone marrow, invades the blood and then other organs. The condition progresses from a stable, more indolent, chronic phase (LEUKEMIA, MYELOID, CHRONIC PHASE) lasting up to 7 years, to an advanced phase composed of an accelerated phase (LEUKEMIA, MYELOID, ACCELERATED PHASE) and BLAST CRISIS.
  1
 

Myelogenous Leukemia -- See Leukemia, Myeloid


Form of leukemia characterized by an uncontrolled proliferation of the myeloid lineage and their precursors (MYELOID PROGENITOR CELLS) in the bone marrow and other sites.
  1
 

Myelogenous Leukemia Chronic -- See Leukemia, Myelogenous, Chronic, BCR-ABL Positive


Clonal hematopoetic disorder caused by an acquired genetic defect in PLURIPOTENT STEM CELLS. It starts in MYELOID CELLS of the bone marrow, invades the blood and then other organs. The condition progresses from a stable, more indolent, chronic phase (LEUKEMIA, MYELOID, CHRONIC PHASE) lasting up to 7 years, to an advanced phase composed of an accelerated phase (LEUKEMIA, MYELOID, ACCELERATED PHASE) and BLAST CRISIS.
  1
 

Myeloid Leukemia -- See Leukemia, Myeloid


Form of leukemia characterized by an uncontrolled proliferation of the myeloid lineage and their precursors (MYELOID PROGENITOR CELLS) in the bone marrow and other sites.
  1
 

Myeloid Leukemia Chronic -- See Leukemia, Myelogenous, Chronic, BCR-ABL Positive


Clonal hematopoetic disorder caused by an acquired genetic defect in PLURIPOTENT STEM CELLS. It starts in MYELOID CELLS of the bone marrow, invades the blood and then other organs. The condition progresses from a stable, more indolent, chronic phase (LEUKEMIA, MYELOID, CHRONIC PHASE) lasting up to 7 years, to an advanced phase composed of an accelerated phase (LEUKEMIA, MYELOID, ACCELERATED PHASE) and BLAST CRISIS.
  1
 

Myeloma Plasma Cell -- See Multiple Myeloma


A malignancy of mature PLASMA CELLS engaging in monoclonal immunoglobulin production. It is characterized by hyperglobulinemia, excess Bence-Jones proteins (free monoclonal IMMUNOGLOBULIN LIGHT CHAINS) in the urine, skeletal destruction, bone pain, and fractures. Other features include ANEMIA; HYPERCALCEMIA; and RENAL INSUFFICIENCY.
  1
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