Muscle Disorders Update [ACTUALIZACIÓN MÉDICO-CONTINUADA EN GENÉTICA APLICADA || NUEVO TÓPICO DE SALUD 2016]

Muscle Disorders Update

Muscle Disorders Update

MedlinePlus sent this bulletin at 04/15/2016 01:11 PM EDT

New on the MedlinePlus Muscle Disorders page:

Genetics Home Reference: phosphoglycerate kinase deficiency

04/13/2016 02:39 PM EDT

Source: National Library of Medicine - 

Genetics Home Reference: inclusion body myopathy with early-onset Paget disease and frontotemporal dementia

04/13/2016 02:39 PM EDT

Source: National Library of Medicine - 

Genetics Home Reference: hereditary myopathy with early respiratory failure

04/13/2016 02:39 PM EDT

Source: National Library of Medicine - 

Genetics Home Reference: hypokalemic periodic paralysis

04/13/2016 02:39 PM EDT

Source: National Library of Medicine - 

Genetics Home Reference: paramyotonia congenita

04/13/2016 02:39 PM EDT

Source: National Library of Medicine - 

Genetics Home Reference: phosphoglycerate mutase deficiency

04/13/2016 02:39 PM EDT

Source: National Library of Medicine - 

Genetics Home Reference: potassium-aggravated myotonia

04/13/2016 02:39 PM EDT

Source: National Library of Medicine - 

Genetics Home Reference: nemaline myopathy

04/13/2016 02:39 PM EDT

Source: National Library of Medicine - 

Genetics Home Reference: inclusion body myopathy 2

04/13/2016 02:39 PM EDT

Source: National Library of Medicine - 

Genetics Home Reference: fibrodysplasia ossificans progressiva

04/13/2016 02:39 PM EDT

Source: National Library of Medicine - 

Genetics Home Reference: multiminicore disease

04/13/2016 02:39 PM EDT

Source: National Library of Medicine - 

Genetics Home Reference: isolated hyperCKemia

04/13/2016 02:39 PM EDT

Source: National Library of Medicine - 

Genetics Home Reference: hyperkalemic periodic paralysis

04/13/2016 02:39 PM EDT

Source: National Library of Medicine - 

Genetics Home Reference: myopathy with deficiency of iron-sulfur cluster assembly enzyme

04/13/2016 02:39 PM EDT

Source: National Library of Medicine - 

Genetics Home Reference: lactate dehydrogenase deficiency

04/13/2016 02:39 PM EDT

Source: National Library of Medicine - 

Genetics Home Reference: glycogen storage disease type VII

04/13/2016 02:39 PM EDT

Source: National Library of Medicine - 

Genetics Home Reference: tubular aggregate myopathy

04/13/2016 02:39 PM EDT

Source: National Library of Medicine - 

Genetics Home Reference: malignant hyperthermia

04/13/2016 02:39 PM EDT

Source: National Library of Medicine - 

Genetics Home Reference: glycogen storage disease type III

04/13/2016 02:39 PM EDT

Source: National Library of Medicine - 

Genetics Home Reference: myotonia congenita

04/13/2016 02:39 PM EDT

Source: National Library of Medicine - 

Genetics Home Reference: rippling muscle disease

04/13/2016 02:39 PM EDT

Source: National Library of Medicine - 

Genetics Home Reference: myostatin-related muscle hypertrophy

04/13/2016 02:39 PM EDT

Source: National Library of Medicine - 

Genetics Home Reference: myosin storage myopathy

04/13/2016 02:39 PM EDT

Source: National Library of Medicine - 

Genetics Home Reference: glycogen storage disease type 0

04/13/2016 02:39 PM EDT

Source: National Library of Medicine - 

Genetics Home Reference: glycogen storage disease type IX

04/13/2016 02:39 PM EDT

Source: National Library of Medicine - 

Genetics Home Reference: neutral lipid storage disease with myopathy

04/13/2016 02:39 PM EDT

Source: National Library of Medicine - 

Genetics Home Reference: intranuclear rod myopathy

04/13/2016 02:39 PM EDT

Source: National Library of Medicine - 

Genetics Home Reference: cap myopathy

04/13/2016 02:39 PM EDT

Source: National Library of Medicine - 

Genetics Home Reference: adenosine monophosphate deaminase deficiency

04/13/2016 02:39 PM EDT

Source: National Library of Medicine - 

Genetics Home Reference: collagen VI-related myopathy

04/13/2016 02:39 PM EDT

Source: National Library of Medicine - 

Genetics Home Reference: congenital fiber-type disproportion

04/13/2016 02:39 PM EDT

Source: National Library of Medicine - 

Genetics Home Reference: distal myopathy 2

04/13/2016 02:39 PM EDT

Source: National Library of Medicine - 

Genetics Home Reference: congenital contractural arachnodactyly

04/13/2016 02:39 PM EDT

Source: National Library of Medicine - 

Genetics Home Reference: centronuclear myopathy

04/13/2016 02:39 PM EDT

Source: National Library of Medicine - 

Genetics Home Reference: actin-accumulation myopathy

04/13/2016 02:39 PM EDT

Source: National Library of Medicine - 

Genetics Home Reference: central core disease

04/13/2016 02:39 PM EDT

Source: National Library of Medicine -