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Abbreviation: LGMD
Appearance Frequency: 362 time(s)
Long forms: 8

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Long Form No. Long Form Research Area Co-occurring Abbreviation PubMed/MEDLINE Info. (Year, Title)
limb-girdle muscular dystrophy
(305 times)
Neurology
(138 times)
DMD (28 times)
BMD (19 times)
CK (14 times)
1984 Genetic counseling in Becker type X-linked muscular dystrophy. II: Practical considerations.
lobula giant movement detector
(34 times)
Neurology
(24 times)
DCMD (9 times)
CPG (1 time)
EMD (1 time)
1976 The neuronal basis of a sensory analyser, the acridid movement detector system. II. response decrement, convergence, and the nature of the excitatory afferents to the fan-like dendrites of the LGMD.
limb-girdle
(9 times)
Neurology
(2 times)
MD (2 times)
AAR (1 time)
ALD (1 time)
1981 Muscle and serum enzymes and isoenzymes in muscular dystrophies.
Limb-Girdle Muscular Dystrophies
(5 times)
Neurology
(2 times)
DMD (2 times)
AD (1 time)
AR (1 time)
2007 Ins and outs of therapy in limb girdle muscular dystrophies.
limb-girdle MD
(4 times)
Neurology
(2 times)
MD (2 times)
A6MCT (1 time)
AAV (1 time)
2001 Secondary calpain3 deficiency in 2q-linked muscular dystrophy: titin is the candidate gene.
limb-girdle dystrophy
(2 times)
Genetics, Medical
(1 time)
CK (1 time)
1991 Linkage analysis in families with autosomal recessive limb-girdle muscular dystrophy (LGMD) and 6q probes flanking the dystrophin-related sequence.
Lobular Giant Movement Detector neurone
(2 times)
Biology
(2 times)
--- 1976 Neuronal basis of a sensory analyser, the acridid movement detector system. III. Control of response amplitude by tonic lateral inhibition.
limb-girdle form
(1 time)
Genetics, Medical
(1 time)
CK (1 time)
DMD (1 time)
FSH (1 time)
1985 Serum CK-MB activity in progressive muscular dystrophy: is it of nosologic value?