Muscular dystrophy overview: genetics and diagnosisMATHEWS, Katherine D.Neurologic clinics. 2003, Vol 21, Num 4, issn 0733-8619, vi, 795-816 [23 p.]Article

The genetics of inherited macular dystrophiesMICHAELIDES, M; HUNT, D. M; MOORE, A. T et al.Journal of medical genetics. 2003, Vol 40, Num 9, pp 641-650, issn 0022-2593, 10 p.Article

Decreased Expression of Peroxiredoxins in Fuchs' Endothelial DystrophyJURKUNAS, Ula V; RAWE, Ian; BITAR, Maya S et al.Investigative ophthalmology & visual science. 2008, Vol 49, Num 7, pp 2956-2963, issn 0146-0404, 8 p.Article

Case of Sjögren reticular dystrophyMCGIMPSEY, Stuart J; RANKIN, Simon J. A.Archives of ophthalmology (1960). 2007, Vol 125, Num 6, issn 0003-9950, 850Article

Increased Clusterin Expression in Fuchs' Endothelial DystrophyJURKUNAS, Ula V; BITAR, Maya S; RAWE, Ian et al.Investigative ophthalmology & visual science. 2008, Vol 49, Num 7, pp 2946-2955, issn 0146-0404, 10 p.Article

IFT80, which encodes a conserved intraflagellar transport protein, is mutated in Jeune asphyxiating thoracic dystrophyBEALES, Philip L; BLAND, Elizabeth; JOHNSON, Colin et al.Nature genetics. 2007, Vol 39, Num 6, pp 729-731, issn 1061-4036, 3 p.Article

An unusual cause of fingernail dystrophyCOUSEN, P. J; RAMSAY, H. M; GAWKRODGER, D. J et al.Clinical and experimental dermatology (Print). 2012, Vol 37, Num 5, pp 589-590, issn 0307-6938, 2 p.Article

Dystrophie myotonique de Steinart = Myotonic dystrophyJUNIEN, C.Journal de génétique humaine. 1989, Vol 37, Num 1, pp 51-54, issn 0021-7743, 4 p.Article

Linkage analysis in granular corneal dystrophy (Groenouw I), Schnyder's crystalline corneal dystrophy, and Reis-Bücklers's corneal dystrophyKÖMPF, J; RITTER, H; LISCH, W et al.Graefe's archive for clinical and experimental ophthalmology. 1989, Vol 227, Num 6, pp 538-540, issn 0721-832XArticle

Upper vs lower extremity functional loss in neuromuscular diseaseLORD, J. P; PORTWOOD, M. M; FOWLER, W. M et al.Archives of physical medicine and rehabilitation. 1987, Vol 68, Num 1, pp 8-9, issn 0003-9993Article

Survey of patients with granular, lattice, avellino, and Reis-Bücklers corneal dystrophies for mutations in the BIGH3 and gelsolin genesAFSHARI, Nasrin A; MULLALLY, James E; AFSHARI, Mehran A et al.Archives of ophthalmology (1960). 2001, Vol 119, Num 1, pp 16-22, issn 0003-9950Article

Les dystrophies de Groenouw : diagnostic clinique et affinités tinctoriales = Groenouw corneal dystrophy. Clinical diagnosisGOULAY, N; DURAND, L; BOUVIER, R et al.Bulletin des sociétés d'ophtalmologie de France. 1993, Vol 93, Num 3, pp 269-272, issn 0081-1270Article

Immunohistochemical localization of chondroitin sulfate in normal and pathological human muscleBERTOLOTTO, A; PALMUCCI, L; GAGLIANO, A et al.Journal of the neurological sciences. 1986, Vol 73, Num 3, pp 233-244, issn 0022-510XArticle

Pain measurement in reflex sympathetic dystrophy syndromeDAVIDOFF, G; MOREY, K; AMANN, M et al.Pain (Amsterdam). 1988, Vol 32, Num 1, pp 27-34, issn 0304-3959Article

Congenital myotonic dystrophy: incidence, clinical aspects and early prognosisWESSTROM, G; BENSCH, J; SCHOLLIN, J et al.Acta paediatrica scandinavica. 1986, Vol 75, Num 5, pp 849-854, issn 0001-656XArticle

An examination of some factors influencing creatine Kinase in the blood of parients with muscular dystrophyJACKSON, M. J; ROUND, J. M; NEWHAM, D. J et al.Muscle & nerve. 1987, Vol 10, Num 1, pp 15-21, issn 0148-639XArticle

The genetics of muscular dystrophiesHARPER, P. S.Progress in medical genetics. 1985, Vol 6, pp 53-90, issn 0079-6441Article

Norepinephrine in reflex sympathetic dystrophy: an hypothesisECKER, A.The Clinical journal of pain. 1989, Vol 5, Num 4, pp 313-315, issn 0749-8047, 3 p.Article

Detection of Duchenne/Becker muscular dystrophy carriers by densitometric scanningPRIOR, T. W; FRIEDMAN, K. J; SILVERMAN, L. M et al.Clinical chemistry (Baltimore, Md.). 1989, Vol 35, Num 6, pp 1256-1257, issn 0009-9147, 2 p.Article

Future prospectsLACHMANN, P. J.British medical bulletin. 1989, Vol 45, Num 3, pp 819-824, issn 0007-1420Article

Unesterified cholesterol in granular, lattice, and macular dystrophiesRODRIGUES, M. M; KRUTH, H. S; RAJAGOPALAN, S et al.American journal of ophthalmology. 1993, Vol 115, Num 1, pp 112-114, issn 0002-9394Article

Molecular deletion patterns in families from southern France with Duchenne/Becker muscular dystrophiesCLAUSTRES, M; TUFFERY, S; CHEVRON, M.-P et al.Human genetics. 1991, Vol 88, Num 2, pp 179-184, issn 0340-6717Article

DNA deletions and recombinations in the gene locus of X-linked muscular dystrophiesSHIMMOTO, M; TSUJI, A; YANG, R.-C et al.Journal of inherited metabolic disease. 1988, Vol 11, Num 3, pp 324-328, issn 0141-8955Article

Central Areolar Choroidal DystrophyBOON, Camiel J. F; KLEVERING, B. Jeroen; CREMERS, Frans P. M et al.Ophthalmology (Rochester, MN). 2009, Vol 116, Num 4, pp 771-782, issn 0161-6420, 12 p.Article

Electrolysis for corneal opacities in a young patient with superficial variant of granular corneal dystrophy (reis-biicklers corneal dystrophy)KAMOI, Mizuka; MASHIMA, Yukihiko; KAWASHIMA, Motoko et al.American journal of ophthalmology. 2005, Vol 139, Num 6, pp 1139-1140, issn 0002-9394, 2 p.Article