The following pages link to Limb–girdle muscular dystrophy
External toolsShowing 50 items.
View (previous 50 | next 50) (20 | 50 | 100 | 250 | 500)- Kocher–Debre–Semelaigne syndrome (links | edit)
- Muscular dystrophy (links | edit)
- Glycogen storage disease type V (links | edit)
- Glycogen storage disease (links | edit)
- Muscular Dystrophy Association (links | edit)
- Duchenne muscular dystrophy (links | edit)
- Glycogen storage disease type II (links | edit)
- Becker muscular dystrophy (links | edit)
- Limb-girdle (redirect page) (links | edit)
- Erb's muscular dystrophy (redirect page) (links | edit)
- Oculopharyngeal muscular dystrophy (links | edit)
- Fukuyama congenital muscular dystrophy (links | edit)
- Nemaline myopathy (links | edit)
- Muscular Dystrophy Canada (links | edit)
- Facioscapulohumeral muscular dystrophy (links | edit)
- Mitochondrial myopathy (links | edit)
- Periodic paralysis (links | edit)
- Mevalonic acid (links | edit)
- Congenital muscular dystrophy (links | edit)
- Lgmd (redirect page) (links | edit)
- Limb girdle muscular dystrophy (redirect page) (links | edit)
- Inclusion body myositis (links | edit)
- Electromyography (links | edit)
- Prelamin-A/C (links | edit)
- Integrin beta 1 (links | edit)
- FHL1 (links | edit)
- CSRP3 (links | edit)
- Medical genetics of Jews (links | edit)
- List of neuromuscular disorders (links | edit)
- User:Doctorwolfie/sandbox (links | edit)
- User:Lukelahood (links | edit)
- Muscular dystrophies, limb-girdle (redirect page) (links | edit)
- Emery–Dreifuss muscular dystrophy (links | edit)
- Distal myopathy (links | edit)
- The Jerry Lewis MDA Labor Day Telethon (links | edit)
- Mesoangioblast (links | edit)
- Myotonic dystrophy (links | edit)
- Bethlem myopathy (links | edit)
- Stamulumab (links | edit)
- Muscular Dystrophy Community Assistance Research and Education Amendments of 2001 (links | edit)
- LGMD (redirect page) (links | edit)
- Limb-Girdle muscular dystrophy (redirect page) (links | edit)
- Sarepta Therapeutics (links | edit)
- Caveolin 3 (links | edit)
- Myotonic Dystrophy Foundation (links | edit)
- Limb-girdle muscular dystrophies (redirect page) (links | edit)
- Ajit Jain (links | edit)
- Calpain-3 (links | edit)
- Michel Fardeau (links | edit)
- Pseudohypertrophy (links | edit)
- User:Brainist/MeSH articles (links | edit)
- Décrypthon (links | edit)
- Hoffmann syndrome (links | edit)
- Dysferlinopathy (redirect page) (links | edit)
- List of diseases (D) (links | edit)
- Myositis (links | edit)
- Dysferlin (links | edit)
- Camptocormia (links | edit)
- Sunil Pradhan (links | edit)
- Haraldur Ingi Þorleifsson (links | edit)
- Talk:Dysferlinopathy (links | edit)
- User:AlexNewArtBot/HorticultureSearchResult/archive7 (links | edit)
- User:AlexNewArtBot/GeneticsSearchResult/archive2 (links | edit)
- User:AlexNewArtBot/NeuroscienceSearchResult/archive3 (links | edit)
- User:AlexNewArtBot/MedicineSearchResult/archive29 (links | edit)
- User:Northupnorth/Jain Foundation (links | edit)
- User:AlexNewArtBot/ReferencesSearchResult/archive64 (links | edit)
- User:AlexNewArtBot/TestFeedSearchResult/archive124 (links | edit)
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- User:Drsalmanshah165/Books/Medical Misplaced Pages 0-F (links | edit)
- User:Drsalmanshah165/Books/Medical Misplaced Pages 0-G (links | edit)
- User:Drsalmanshah165/Books/Medical Wikipedia0-h (links | edit)
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- User:Drsalmanshah165/Books/Medical Wikipediac0-J (links | edit)
- User:Drsalmanshah165/Books/Medical Misplaced Pages 0-K (links | edit)
- User:Drsalmanshah165/Books/Medical Misplaced Pages 0-L (links | edit)
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- User:Drsalmanshah165/Books/Medical Misplaced Pages 0-N (links | edit)
- User:Drsalmanshah165/Books/Medical Misplaced Pages 0-pha (links | edit)
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- User:Drsalmanshah165/Books/Medical Misplaced Pages 0-U (links | edit)
- User:Drsalmanshah165/Books/Medical Misplaced Pages 0-V (links | edit)
- User:Drsalmanshah165/Books/Medical Misplaced Pages 0-W (links | edit)
- User:Drsalmanshah165/Books/Medical Misplaced Pages 0-X (links | edit)
- User:Drsalmanshah165/Books/Medical Misplaced Pages 0-Y (links | edit)
- User:Drsalmanshah165/Books/Medical Misplaced Pages 0-z (links | edit)
- User:Drsalmanshah165/Books/Medical wikipedia (links | edit)
- User:Drsalmanshah165/Books/Offline Medical Misplaced Pages 0-Z (links | edit)
- User:MastCell/Ignored medical articles (links | edit)
- User:Omer476/Books/List Of Diseases(D) (links | edit)
- User:Omer476/Books/Rare diseases (A-O) (links | edit)
- User:PriceDL/List of all WikiProject Medicine articles (links | edit)
- User:CFCF/sandbox/46 (links | edit)
- User talk:Anandks007/Med (links | edit)
- User talk:Northupnorth (links | edit)
- Misplaced Pages:WikiProject Medicine/Lists of pages/Articles (links | edit)
- Misplaced Pages:WikiProject Medicine/Lists of pages/Low-importance medicine articles (links | edit)
- Misplaced Pages:Articles for creation/Redirects and categories/2014-01 (links | edit)
- Misplaced Pages:WikiProject Medicine/Popular pages En 2013b (links | edit)
- Misplaced Pages:Sockpuppet investigations/Leeer333/Archive (links | edit)
- Limb-Girdle Muscular Dystrophy (redirect page) (links | edit)
- Muskelsvindfonden (links | edit)
- LGMD2A (redirect page) (links | edit)
- Calpainopathy (links | edit)
- Dystrophinopathy (links | edit)
- Limb-girdle muscular dystrophy (redirect page) (links | edit)
- Charcot–Marie–Tooth disease (links | edit)
- Lambert–Eaton myasthenic syndrome (links | edit)
- Muscular dystrophy (links | edit)
- Myasthenia gravis (links | edit)
- Neuromyotonia (links | edit)
- Marfan syndrome (links | edit)
- List of genetic disorders (links | edit)
- Hereditary haemochromatosis (links | edit)
- Glycogen storage disease (links | edit)
- Congenital disorder of glycosylation (links | edit)
- Hereditary spastic paraplegia (links | edit)
- List of diseases (L) (links | edit)
- Cleft lip and cleft palate (links | edit)
- Long QT syndrome (links | edit)
- Limb–girdle muscular dystrophy (links | edit)
- Hereditary spherocytosis (links | edit)
- Arrhythmogenic cardiomyopathy (links | edit)
- Hypertrophic cardiomyopathy (links | edit)
- Dilated cardiomyopathy (links | edit)
- Epidermolytic hyperkeratosis (links | edit)
- Alexander disease (links | edit)
- Usher syndrome (links | edit)
- Duchenne muscular dystrophy (links | edit)
- Hypotonia (links | edit)
- Gardner's syndrome (links | edit)
- Hyperkalemic periodic paralysis (links | edit)
- Becker muscular dystrophy (links | edit)
- Oculopharyngeal muscular dystrophy (links | edit)
- Familial adenomatous polyposis (links | edit)
- Wiskott–Aldrich syndrome (links | edit)
- Palmoplantar keratoderma (links | edit)
- Malouf syndrome (links | edit)
- Fukuyama congenital muscular dystrophy (links | edit)
- Myopathy (links | edit)
- Titin (links | edit)
- Nemaline myopathy (links | edit)
- Caveolin (links | edit)
- Spinocerebellar ataxia (links | edit)
- Channelopathy (links | edit)
- Chédiak–Higashi syndrome (links | edit)
- Facioscapulohumeral muscular dystrophy (links | edit)
- Giant axonal neuropathy (links | edit)
- Myotonia congenita (links | edit)
- Mitochondrial myopathy (links | edit)
- Hereditary elliptocytosis (links | edit)
- Kearns–Sayre syndrome (links | edit)
- Hypertonia (links | edit)
- Walker–Warburg syndrome (links | edit)
- Hypokalemic periodic paralysis (links | edit)
- Paramyotonia congenita (links | edit)
- Chromosome 7 (links | edit)
- Nonsyndromic deafness (links | edit)
- Hermansky–Pudlak syndrome (links | edit)
- Dysferlin (links | edit)
- MELAS syndrome (links | edit)
- Hereditary pyropoikilocytosis (links | edit)
- Choroideremia (links | edit)
- Erb (links | edit)
- Zaspopathy (links | edit)
- Cohen syndrome (links | edit)
- Tauopathy (links | edit)
- Griscelli syndrome (links | edit)
- Neuromuscular disease (links | edit)
- Centronuclear myopathy (links | edit)
- Freeman–Sheldon syndrome (links | edit)
- Sarcoglycanopathy (links | edit)
- Sarcoglycan (links | edit)
- Larsen syndrome (links | edit)
- Epidermolysis bullosa simplex (links | edit)
- Emery–Dreifuss muscular dystrophy (links | edit)
- MERRF syndrome (links | edit)
- Dejerine–Sottas disease (links | edit)
- Short rib–polydactyly syndrome (links | edit)
- Distal myopathy (links | edit)
- Kindler syndrome (links | edit)
- White sponge nevus (links | edit)
- Hemophagocytic lymphohistiocytosis (links | edit)
- MASS syndrome (links | edit)
- Myotonic dystrophy (links | edit)
- Naegeli–Franceschetti–Jadassohn syndrome (links | edit)
- Congenital myopathy (links | edit)
- Laminopathy (links | edit)
- Bethlem myopathy (links | edit)
- Stamulumab (links | edit)
- Monilethrix (links | edit)
- Oguchi disease (links | edit)
- May–Hegglin anomaly (links | edit)
- Congenital contractural arachnodactyly (links | edit)
- Dystrobrevin (links | edit)
- Muscular Dystrophy Community Assistance Research and Education Amendments of 2001 (links | edit)
- Chronic progressive external ophthalmoplegia (links | edit)
- Buschke–Ollendorff syndrome (links | edit)
- Fukutin (links | edit)
- Barraquer–Simons syndrome (links | edit)
- Pelger–Huët anomaly (links | edit)
- Steatocystoma multiplex (links | edit)
- Thyrotoxic myopathy (links | edit)
- Telethonin (links | edit)
- Delta-sarcoglycan (links | edit)
- DNAJB6 (links | edit)
- SGCG (links | edit)
- Obscurin (links | edit)
- POMT1 (links | edit)
- Osteopoikilosis (links | edit)
- TRIM32 (links | edit)
- Weill–Marchesani syndrome (links | edit)
- Central core disease (links | edit)
- Boomerang dysplasia (links | edit)
- Microcephalic osteodysplastic primordial dwarfism type II (links | edit)
- Neuromuscular junction disease (links | edit)
- Elejalde syndrome (links | edit)
- X-linked intellectual disability (links | edit)
- Ichthyosis bullosa of Siemens (links | edit)
- Metabolic myopathy (links | edit)
- FG syndrome (links | edit)
- Ichthyosis hystrix (links | edit)
- Reticular pigmented anomaly of the flexures (links | edit)
- Naxos syndrome (links | edit)
- Mandibuloacral dysplasia (links | edit)
- Keratin disease (links | edit)
- Familial cirrhosis (links | edit)
- Dunnigan familial partial lipodystrophy (links | edit)
- Congenital generalized lipodystrophy (links | edit)
- Familial partial lipodystrophy (links | edit)
- Ullrich congenital muscular dystrophy (links | edit)
- Jean-Christophe Parisot (links | edit)
- X-linked myotubular myopathy (links | edit)
- Terminal osseous dysplasia with pigmentary defects (links | edit)
- Arthrogryposis–renal dysfunction–cholestasis syndrome (links | edit)
- CEDNIK syndrome (links | edit)
- Skin fragility syndrome (links | edit)
- Limb girdle syndrome (links | edit)
- Thyrotoxic periodic paralysis (links | edit)
- Asphyxiating thoracic dysplasia (links | edit)
- Cranio-lenticulo-sutural dysplasia (links | edit)
- Inherited disorders of trafficking (links | edit)
- Surfactant metabolism dysfunction (links | edit)
- Desmin-related myofibrillar myopathy (links | edit)
- Familial exudative vitreoretinopathy (links | edit)
- Myopathy, X-linked, with excessive autophagy (links | edit)
- Electromyoneurography (links | edit)
- Paul D. Wellstone Muscular Dystrophy Community Assistance, Research and Education Amendments of 2013 (links | edit)
- Innate resistance to HIV (links | edit)
- List of acts of the 107th United States Congress (links | edit)
- Ferlins (links | edit)
- List of ICD-9 codes 320–389: diseases of the nervous system and sense organs (links | edit)
- Calpainopathy (links | edit)
- Halperin-Birk syndrome (links | edit)
- Transient neonatal myasthenia gravis (links | edit)
- Talk:Limb-girdle muscular dystrophy (transclusion) (links | edit)
- User:Davidruben/OrphaNet (links | edit)
- User:Northupnorth/dysferlinopathy (links | edit)
- User:Northupnorth/Jain Foundation (links | edit)
- User:Paul (Cripaul) James (links | edit)
- User:NussPoyava/sandbox (links | edit)
- User:Odeyaka/sandbox (links | edit)
- User:Chirocare13/Books/DACNB EXAM LIST (links | edit)
- User:Drsalmanshah165/Books/Medical Misplaced Pages (links | edit)
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- User:MastCell/Ignored medical articles (links | edit)
- User:Carolina2904/sandbox (links | edit)
- User:Daniel Mietchen/Wikidata lists/Items with MeSH Codes (links | edit)
- User:EranBot/Copyright/6 (links | edit)
- User:Janeannyoung/sandbox (links | edit)
- User:Cjcolon723/sandbox (links | edit)
- User:CFR13/Books/Neurological Disorders (links | edit)
- User:PriceDL/List of all WikiProject Medicine articles (links | edit)
- User:CFCF/sandbox/46 (links | edit)
- User:Evaldez03/sandbox (links | edit)
- User:Jgfriedman99 (links | edit)
- User:Y-S.Ko/Wikipedia course/Diseases (links | edit)
- User:Lukelahood/sandbox (links | edit)
- User:Yaqi Zhao/sandbox/Channelopathy/skeleton muscle (links | edit)
- User:NuriHalperin/sandbox (links | edit)
- User:MiaSH/Tauopathy (links | edit)
- User talk:Anandks007/Med (links | edit)
- User talk:AmberSmit98765 (links | edit)
- Misplaced Pages:WikiProject Spam/LinkReports/nema.be (links | edit)
- Misplaced Pages:WikiProject Medicine/Lists of pages/Low-importance medicine articles (links | edit)
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- Misplaced Pages:WikiProject Short descriptions/wd/diseases (links | edit)
- Misplaced Pages talk:WikiProject Medicine/Archive 78 (links | edit)
- Template:Diseases of myoneural junction and muscle (links | edit)
- Template:Vesicular transport protein disorders (links | edit)
- Template:Cytoskeletal defects (links | edit)
- Template:Other cell membrane protein disorders (links | edit)
- Template:Infobox medical condition/testcases (links | edit)
- David Gardner-Medwin (links | edit)
- Matilda Feyiṣayọ Ibini (links | edit)
- Pseudoathletic appearance (links | edit)
- Beta-sarcoglycanopathy (redirect page) (links | edit)
- Muscular dystrophy limb-girdle autosomal dominant (redirect to section "Types") (links | edit)
- Muscular dystrophy limb-girdle type 2B, Myoshi type (redirect to section "Types") (links | edit)
- Muscular dystrophy Hutterite type (redirect to section "Types") (links | edit)