J. Fine

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The risk of cardiomyopathy in inherited epidermolysis bullosa

C. Suchindran, M. Hall, J. Fine, 2008, The British journal of dermatology.

The genetic basis of Weber-Cockayne epidermolysis bullosa simplex.

E. Fuchs, Q. Yu, Y. Chan, 1993, Proceedings of the National Academy of Sciences of the United States of America.

Consensus reclassification of inherited epidermolysis bullosa and other disorders with skin fragility

C. Bodemer, J. Uitto, J. McGrath, 2020, The British journal of dermatology.

Structural and compositional alteration of tooth enamel in hereditary epidermolysis bullosa.

J. T. Wright, J. Fine, K. Hall, 1996, Connective tissue research.

Oral involvement of recessive dystrophic epidermolysis bullosa inversa.

J. T. Wright, J. Fine, L. Johnson, 1993, American journal of medical genetics.

The genetic basis of epidermolysis bullosa simplex with mottled pigmentation.

E. Fuchs, P. Coulombe, T. Gedde-Dahl, 1996, Proceedings of the National Academy of Sciences of the United States of America.

Dental caries risk in hereditary epidermolysis bullosa.

J. T. Wright, J. Fine, L. Johnson, 1994, Pediatric dentistry.

Development defects of enamel in humans with hereditary epidermolysis bullosa.

J. T. Wright, J. Fine, L. Johnson, 1993, Archives of oral biology.

Hereditary epidermolysis bullosa: oral manifestations and dental management.

J. T. Wright, J. Fine, L. Johnson, 1993, Pediatric dentistry.

HLA and epidermolysis bullosa. Association between the HLA complex and recessive dystrophic epidermolysis bullosa.

S. Tyring, J. Fine, S. Vaidya, 1991, Archives of dermatology.

Management of cutaneous squamous cell carcinoma in patients with epidermolysis bullosa: best clinical practice guidelines

J. McGrath, D. Murrell, A. Diem, 2016, The British journal of dermatology.

Impact of inherited epidermolysis bullosa on parental interpersonal relationships, marital status and family size

C. Suchindran, J. Fine, J. Fine, 2005, The British journal of dermatology.

Assessment of mobility, activities and pain in different subtypes of epidermolysis bullosa

C. Suchindran, J. Fine, M. Weiner, 2004, Clinical and experimental dermatology.

Association Between the HLA Complex and Recessive Dystrophic Epidermolysis Bullosa

S. Tyring, J. Fine, S. Vaidya, 2017 .

Natural killer cell activity is reduced in patients with severe forms of inherited epidermolysis bullosa.

S. Tyring, J. Fine, V. Chopra, 1989, Archives of dermatology.

Salivary function of persons with hereditary epidermolysis bullosa.

K. Evans, J. T. Wright, N. Childers, 1991, Oral surgery, oral medicine, and oral pathology.

Pyoderma gangrenosum associated with primary biliary cirrhosis.

J. Hoofnagle, G. Minuk, J. Fine, 1983, Archives of internal medicine.

Pemphigus Vulgaris: Combined Treatment With Intravenous Corticosteroid Pulse Therapy, Plasmapheresis, and Azathioprine

L. Green, J. Fine, M. Appell, 1988 .

Remission of severe epidermolysis bullosa acquisita induced by extracorporeal photochemotherapy

J. Miller, D. Ellis, L. King, 1995, The British journal of dermatology.

Pemphigus vulgaris. Combined treatment with intravenous corticosteroid pulse therapy, plasmapheresis, and azathioprine.

L. Green, J. Fine, M. Appell, 1988, Archives of dermatology.

Oral soft tissues in hereditary epidermolysis bullosa.

J. T. Wright, J. Fine, L. Johnson, 1991, Oral surgery, oral medicine, and oral pathology.

Immunohistochemical, ultrastructural, and molecular features of Kindler syndrome distinguish it from dystrophic epidermolysis bullosa.

R. Burgeson, H. Shimizu, T. Nishikawa, 1997, Archives of dermatology.

Applicability of 19–DEJ‐l monoclonal antibody for the prenatal diagnosis or exclusion of junctional epidermolysis bullosa

K. Holbrook, S. Elias, J. Fine, 1990, Prenatal diagnosis.

Epidermolysis bullosa Cardiomyopathy in inherited

C. Suchindran, M. Hall, J. Fine, 2018 .

CT sialography: utilising acinar filling.

K. Evers, L. Moss, J. Zito, 1985, British Journal of Radiology.

HLA and epidermolysis bullosa: evidence for independent assortment of Weber-Cockayne subtype of epidermolysis bullosa and HLA complex.

S. Tyring, J. Fine, M. Feldkamp, 1991, Journal of dermatological science.

Peripheral blood mononuclear cell subsets in patients with severe inherited forms of epidermolysis bullosa.

S. Tyring, J. Fine, V. Chopra, 1992, Archives of dermatology.

The National Epidermolysis Bullosa Registry basic demographic characteristics of a prospective multicenter project

R. Stern, E. Bauer, V. Sybert, 1994 .

Defective in vivo expression and apparently normal in vitro expression of a newly identified 105‐kDa lower lamina lucida protein in dystrophic epidermolysis bullosa

E. Bauer, K. Cooper, L. Chan, 1995, The British journal of dermatology.

Hereditary epidermolysis bullosa.

J. T. Wright, J. Fine, 1994, Seminars in Dermatology.

Risk of skin cancers and inherited epidermolysis bullosa (EB) — Determination of differences across major EB subtypes. As assessed by lifetable analysis technique JQ

R. Stern, E. Bauer, V. Sybert, 1994 .

Epidermolysis bullosa simplex superficialis. A new variant of epidermolysis bullosa characterized by subcorneal skin cleavage mimicking peeling skin syndrome.

J. Fine, J. Fine, L. Johnson, 1989, Archives of dermatology.