J. Fine

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Remission of severe epidermolysis bullosa acquisita induced by extracorporeal photochemotherapy

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

Letter: Multiple myeloma and renal impairment.

R. Luke, J. Fine, E. D. Rees, 1973, Lancet.

Genetic Disorders Predisposing to Skin Malignancy

J. Fine, C. Schadt, 2011 .

In utero development of epidermolysis bullosa acquisita

J. Fine, A. Boyd, Brandon Danford, 2018, Pediatric dermatology.

The classification of inherited epidermolysis bullosa (EB): Report of the Third International Consensus Meeting on Diagnosis and Classification of EB.

E. Bauer, H. Shimizu, J. Uitto, 2008, Journal of the American Academy of Dermatology.

Structure and antigenicity of the skin basement membrane zone

J. Fine, 1991, Journal of cutaneous pathology.

The TORCH syndrome: a clinical review.

K. Arndt, J. Fine, Kenneth A. Arndt, 1985, Journal of the American Academy of Dermatology.

Gastrointestinal Complications of Inherited Epidermolysis Bullosa: Cumulative Experience of the National Epidermolysis Bullosa Registry

C. Suchindran, J. Fine, M. Weiner, 2008, Journal of pediatric gastroenterology and nutrition.

Nephrogenic systemic fibrosis: report of an additional case with granulomatous inflammation.

J. L. Abraham, J. Fine, C. Wilford, 2010, The American Journal of dermatopathology.

Genetic Blistering Diseases

J. Fine, S. Burge, R. Eady, 2008 .

Epidermolysis bullosa carrier frequencies in the US population.

J. Uitto, J. Fine, E. Pfendner, 2001, The Journal of investigative dermatology.

Revised clinical and laboratory criteria for subtypes of inherited epidermolysis bullosa. A consensus report by the Subcommittee on Diagnosis and Classification of the National Epidermolysis Bullosa Registry.

E. Bauer, K. Holbrook, R. Pearson, 1991, Journal of the American Academy of Dermatology.

Gingival telangiectases: an underappreciated physical sign of juvenile dermatomyositis.

J. Fine, L. Stein, D. McCauliffe, 1999, Archives of dermatology.

Kindler Syndrome: Report of Two Cases and Review of the Literature

Y. Horiguchi, M. Duvic, J. Fine, 1989, Pediatric dermatology.

Inherited epidermolysis bullosa: past, present, and future

J. Fine, 2010, Annals of the New York Academy of Sciences.

Autosomal recessive epidermolysis bullosa simplex. Generalized phenotypic features suggestive of junctional or dystrophic epidermolysis bullosa, and association with neuromuscular diseases.

H. Bock, Y. Horiguchi, J. Fine, 1989, Archives of dermatology.

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.

ReviewInherited epidermolysis bullosa

J. Fine, 2015 .

Inherited epidermolysis bullosa

J. Fine, 2010, Orphanet journal of rare diseases.

Extracutaneous manifestations and complications of inherited epidermolysis bullosa: part I. Epithelial associated tissues.

J. Mellerio, J. Fine, 2009, Journal of the American Academy of Dermatology.

Extracutaneous manifestations and complications of inherited epidermolysis bullosa: part II. Other organs.

J. Mellerio, J. Fine, 2009, Journal of the American Academy of Dermatology.

Changing clinical and laboratory concepts in inherited epidermolysis bullosa.

J. Fine, 1988, Archives of dermatology.

Pathology and Pathogenesis of Epidermolysis Bullosa

J. Fine, 1992 .

Epidermolysis Bullosa

J. Fine, 1986, International journal of dermatology.

Epidermolysis Bullosa Simplex: Identification of a Kindred with Autosomal Recessive Transmission of the Weher‐Cockayne Variety

Y. Horiguchi, J. Fine, L. Johnson, 1989, Pediatric dermatology.

A specific defect in glycosylation of epidermal cell membranes. Definition in skin from patients with epidermolysis bullosa simplex.

R. D. Griffith, J. Fine, 1985, Archives of dermatology.

Inherited epidermolysis bullosa and the risk of death from renal disease: experience of the National Epidermolysis Bullosa Registry.

C. Suchindran, J. Fine, M. Weiner, 2004, American journal of kidney diseases : the official journal of the National Kidney Foundation.

Eye involvement in inherited epidermolysis bullosa: experience of the National Epidermolysis Bullosa Registry.

C. Suchindran, J. Fine, M. Weiner, 2004, American journal of ophthalmology.

19-DEJ-1, a hemidesmosome-anchoring filament complex-associated monoclonal antibody. Definition of a new skin basement membrane antigenic defect in junctional and dystrophic epidermolysis bullosa.

J. Couchman, Y. Horiguchi, J. Fine, 1989, Archives of dermatology.

The National Epidermolysis Bullosa Registry.

C. Suchindran, J. Fine, L. Johnson, 1994, The Journal of investigative dermatology.

Epidermolysis Bullosa

J. McGrath, I. Chapple, C. Has, 2020, Braun-Falco´s Dermatology.

Increased frequency of HLA-DR2 in patients with autoantibodies to epidermolysis bullosa acquisita antigen: evidence that the expression of autoimmunity to type VII collagen is HLA class II allele associated.

D. Woodley, R. Briggaman, J. Fine, 1988, The Journal of investigative dermatology.

Epitope mapping of the laminin molecule in murine skin basement membrane zone: demonstration of spatial differences in ultrastructural localization.

D. Abrahamson, Y. Horiguchi, J. Fine, 1991, The Journal of investigative dermatology.

Mastocytosis

J. Fine, 1980 .

KF-1 monoclonal antibody defines a specific basement membrane antigen defect in dystrophic forms of epidermolysis bullosa.

S. Katz, J. Fine, H. Hintner, 1984, The Journal of investigative dermatology.

Ultrastructural localization of the core protein of a basement membrane-specific chondroitin sulfate proteoglycan in adult rat skin

J. Couchman, Y. Horiguchi, K. McCarthy, 2004, Archives of Dermatological Research.

RENAL CYTOTOXIC EFFECTS OF BENCE-JONES PROTEIN

J. Fine, E. D. Rees, 1977, The Lancet.

Detection and partial characterization of a midlamina lucida-hemidesmosome-associated antigen (19-DEJ-1) present within human skin.

J. Jester, J. Couchman, Y. Horiguchi, 1989, The Journal of investigative dermatology.

LDA-1: a ubiquitous noncollagenous lamina densa component of basement membrane detected by monoclonal antibody technique.

S. Gay, J. Fine, 1986, The Journal of investigative dermatology.

Monoclonal antibodies and the skin biopsy: current and potential clinical applications.

J. Fine, 1985, The American journal of the medical sciences.

The appearance of four basement membrane zone antigens in developing human fetal skin.

K. Holbrook, S. Katz, J. Fine, 1984, The Journal of investigative dermatology.

Squamous cell carcinoma and junctional epidermolysis bullosa.

J. Fine, 2012, Journal of the American Academy of Dermatology.

A mouse model of generalized non-Herlitz junctional epidermolysis bullosa.

J. Sundberg, J. Bubier, D. Roopenian, 2010, The Journal of investigative dermatology.

Lamina densa malformation involved in histogenesis of primary localized cutaneous amyloidosis.

I. Leigh, T. Yoshiki, Y. Horiguchi, 1992, The Journal of investigative dermatology.

Distribution, ultrastructural localization, and ontogeny of the core protein of a heparan sulfate proteoglycan in human skin and other basement membranes.

A. Ljubimov, J. Couchman, Y. Horiguchi, 1989, The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society.

Clinical Manifestations and Complications

M. Laimer, J. Stoiber, J. Fine, 2009 .

Characterization and isolation of poly- and monoclonal antibodies against collagen for use in immunohistochemistry.

S. Gay, J. Fine, 1987, Methods in enzymology.

A unique presentation of calcinosis cutis in a patient with cystic fibrosis after double lung transplants.

J. Woosley, J. Fine, J. Friedman, 2003, Journal of the American Academy of Dermatology.

The first international consensus on mucous membrane pemphigoid: definition, diagnostic criteria, pathogenic factors, medical treatment, and prognostic indicators.

D. West, D. Zillikens, K. Yancey, 2002, Archives of dermatology.

Drug-induced linear IgA bullous dermatosis in a patient with a vancomycin-impregnated cement spacer.

E. Tkaczyk, J. Zic, J. Powers, 2018, Cutis.

Neutrophilic Eccrine Hidradenitis: A Distinctive Type of Neutrophilic Dermatosis Associated With Myelogenous Leukemia and Chemotherapy

M. Mihm, G. Murphy, J. Fine, 1982 .

Cutaneous lesions in disseminated candidiasis mimicking ecthyma gangrenosum.

J. Miller, J. Fine, H. Haynes, 1981, The American journal of medicine.

Canine epidermolysis bullosa acquisita: circulating autoantibodies target the aminoterminal non-collagenous (NC1) domain of collagen VII in anchoring fibrils.

Dawn A. D. Chasse, N. Monteiro-Riviere, Mei Chen, 1998, Veterinary dermatology.

Autoimmune bullous diseases with skin and eye involvement: Cicatricial pemphigoid, pemphigus vulgaris, and pemphigus paraneoplastica.

J. Thorne, J. Fine, A. Moradi, 2016, Clinics in dermatology.

Immunofluorescence on split skin for the detection and differentiation of basement membrane zone autoantibodies.

R. Briggaman, M. Forbes, J. Fine, 1992, Journal of the American Academy of Dermatology.

Identification and partial characterization of a novel 105-kDalton lower lamina lucida autoantigen associated with a novel immune-mediated subepidermal blistering disease.

D. Woodley, R. Briggaman, K. Cooper, 1993, The Journal of investigative dermatology.

Immunoelectron microscopy and immunofluorescence antigenic mapping: diagnostic applications.

Y. Horiguchi, J. Fine, Jo-David Fine, 1991, Clinics in dermatology.

Bullous systemic lupus erythematosus: an unusual clinical course and detectable circulating autoantibodies to the epidermolysis bullosa acquisita antigen.

J. Fine, W. Gammon, W. M. Sams, 1986, Journal of the American Academy of Dermatology.

Immunofluorescence and immunoelectron microscopic studies in cicatricial pemphigoid.

S. Katz, J. Fine, G. Neises, 1984, The Journal of investigative dermatology.

The presence of intra-lamina lucida blister formation in epidermolysis bullosa acquisita: possible role of leukocytes.

S. Tyring, J. Fine, W. Gammon, 1989, The Journal of investigative dermatology.

Linear IgA bullous dermatosis v dermatitis herpetiformis. Quantitative measurements of dermoepidermal alterations.

M. Mihm, G. Murphy, J. Fine, 1984, Archives of dermatology.

Antigenic features and structural correlates of basement membranes. Relationship to epidermolysis bullosa.

J. Fine, JD Fine, 1988, Archives of dermatology.

Epidermolysis bullosa: variability of expression of cicatricial pemphigoid, bullous pemphigoid, and epidermolysis bullosa acquisita antigens in clinically uninvolved skin.

J. Fine, Jo-David Fine, 1985, The Journal of investigative dermatology.

Management of acquired bullous skin diseases.

J. Fine, 1995, The New England journal of medicine.

Persistent subepidermal blistering in split-thickness skin graft sites. Ultrastructural and antigenic features simulating dystrophic or immunofluorescence-negative acquired epidermolysis bullosa.

A. Solomon, J. Fine, R. Sánchez, 1988, Archives of dermatology.

Psychiatric reaction to dapsone and sulfapyridine.

M. Donahue, S. Katz, J. Fine, 1983, Journal of the American Academy of Dermatology.

Erythematous plaques and papules on a premature infant.

J. Weitkamp, E. Tkaczyk, Rachel Redenius, 2017, Journal of the American Academy of Dermatology.

Cicatricial pemphigoid, bullous pemphigoid, and epidermolysis bullosa acquisita antigens: differences in organ and species specificities and localization in chemically-separated human skin of three basement membrane antigens.

J. Fine, 1985, Collagen and related research.

Revised classification system for inherited epidermolysis bullosa: Report of the Second International Consensus Meeting on diagnosis and classification of epidermolysis bullosa.

E. Bauer, H. Shimizu, J. Uitto, 2000, Journal of the American Academy of Dermatology.

Cutaneous Leukocytoclastic Vasculitis in the Rose Spot of Paratyphoid Fever

J. Fine, T. Harrist, Terence J. Harrist, 1982, International journal of dermatology.

Genetic basis of dominantly inherited transient bullous dermolysis of the newborn: a splice site mutation in the type VII collagen gene.

J. Uitto, A. Christiano, J. Fine, 1997, The Journal of investigative dermatology.

Tracheolaryngeal Complications of Inherited Epidermolysis Bullosa: Cumulative Experience of the National Epidermolysis Bullosa Registry

C. Suchindran, J. Fine, M. Weiner, 2007, The Laryngoscope.

Inherited epidermolysis bullosa: updated recommendations on diagnosis and classification.

E. Bauer, H. Shimizu, J. Uitto, 2014, Journal of the American Academy of Dermatology.

Herpes gestationis. Persistent disease activity 11 years post partum.

J. Fine, E. Omura, 1985, Archives of dermatology.

Phaeohyphomycosis caused by Rhytidhysteron rufulum

J. Fine, A. Boyd, J. Braue, 2019, Clinical and experimental dermatology.

Inherited epidermolysis bullosa comes into the new millenium: a revised classification system based on current knowledge of pathogenetic mechanisms and the clinical, laboratory, and epidemiologic findings of large, well-defined patient cohorts.

J. McGrath, J. Fine, R. Eady, 2000, Journal of the American Academy of Dermatology.

Absent expression of collagen XVII (BPAG2, BP180) in canine familial localized junctional epidermolysis bullosa.

J. Ortonne, T. Olivry, J. Fine, 1997, Veterinary dermatology.

Inherited epidermolysis bullosa: recent basic and clinical advances

J. Fine, 2010, Current opinion in pediatrics.

Genitourinary complications of inherited epidermolysis bullosa: experience of the national epidermylosis bullosa registry and review of the literature.

C. Suchindran, J. Fine, Jo-David Fine, 2004, The Journal of urology.

Epidermolysis Bullosa

J. Fine, 2007, Annals of the New York Academy of Sciences.

GB3 monoclonal antibody for the diagnosis of junctional epidermolysis bullosa: results of a multicenter study.

J. Ortonne, P. Verrando, R. Eady, 1990, Journal of the American Academy of Dermatology.

Intraepidermal type VII collagen

I. Leigh, Y. Horiguchi, J. Fine, 1990 .

Blood vitamin and trace metal levels in epidermolysis bullosa.

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

The generalized atrophic benign form of junctional epidermolysis bullosa. Experience with four patients in the United States.

A. Paller, J. Fine, R. Pearson, 1986, Archives of dermatology.

Distinctive eruption characterized by linear supravenous papules and erythroderma following broxuridine (bromodeoxyuridine) therapy and radiotherapy.

J. Fine, S. Breathnach, 1986, Archives of dermatology.

Epidermolysis bullosa and the risk of life-threatening cancers: the National EB Registry experience, 1986-2006.

C. Suchindran, J. Fine, M. Weiner, 2009, Journal of the American Academy of Dermatology.

Cause-specific risks of childhood death in inherited epidermolysis bullosa.

C. Suchindran, J. Fine, M. Weiner, 2008, The Journal of pediatrics.

Pseudosyndactyly and Musculoskeletal Contractures in Inherited Epidermolysis Bullosa: Experience of the National Epidermolysis Bullosa Registry, 1986–2002

C. Suchindran, J. Fine, M. Weiner, 2005, Journal of hand surgery.

Possible role for sentinal node biopsy in the management of squamous cell carcinomas in inherited epidermolysis bullosa.

J. Fine, 2004, Archives of dermatology.

Chemoprevention of squamous cell carcinoma in recessive dystrophic epidermolysis bullosa: results of a phase 1 trial of systemic isotretinoin.

C. Suchindran, J. Fine, M. Weiner, 2004, Journal of the American Academy of Dermatology.

Systemic granulocyte colony-stimulating factor (G-CSF) enhances wound healing in dystrophic epidermolysis bullosa (DEB): Results of a pilot trial.

H. Frangoul, J. Fine, B. Manes, 2015, Journal of the American Academy of Dermatology.

The DEBRA International Visioning/Consensus Meeting on Epidermolysis Bullosa: summary and recommendations.

J. Uitto, J. Fine, R. Eady, 2000, The Journal of investigative dermatology.

Urethral meatal stenosis in junctional epidermolysis bullosa: a rare complication effectively treated with a novel and simple modality

D. Murrell, O. Wargon, A. Rubin, 2007, International journal of dermatology.

Patients with severe forms of inherited epidermolysis bullosa exhibit decreased lymphokine and monokine production

S. Tyring, J. Fine, V. Chopra, 1990, Journal of Clinical Immunology.

Tetracycline and epidermolysis bullosa simplex: a new indication for one of the oldest and most widely used drugs in dermatology?

J. Fine, R. Eady, 1999, Archives of dermatology.

Skin bioequivalents and their role in the treatment of inherited epidermolysis bullosa.

J. Fine, 2000, Archives of dermatology.

Entactin: ultrastructural localization of an ubiquitous basement membrane glycoprotein in mouse skin

A. Ljubimov, J. Couchman, Y. Horiguchi, 2004, Archives of Dermatological Research.

Alpha‐fetoprotein and acetylcholinesterase are not predictive of fetal junctional epidermolysis bullosa, Herlitz variant

K. Holbrook, L. Shulman, S. Elias, 1991, Prenatal diagnosis.

19-DEJ-1, a monoclonal antibody to the hemidesmosome-anchoring filament complex, is the only reliable immunohistochemical probe for all major forms of junctional epidermolysis bullosa.

J. Fine, 1990, Archives of dermatology.

Chondroitin 6-sulfate proteoglycan but not heparan sulfate proteoglycan is abnormally expressed in skin basement membrane from patients with dominant and recessive dystrophic epidermolysis bullosa.

J. Couchman, J. Fine, 1989, The Journal of investigative dermatology.

Prenatal diagnosis of dominant and recessive dystrophic epidermolysis bullosa: application and limitations in the use of KF-1 and LH 7:2 monoclonal antibodies and immunofluorescence mapping technique.

K. Holbrook, R. Carpenter, J. Hejtmancik, 1988, The Journal of investigative dermatology.

Efficacy of systemic phenytoin in the treatment of junctional epidermolysis bullosa.

J. Fine, L. Johnson, 1988, Archives of dermatology.

Chondroitin-6-sulfate-containing proteoglycan: a new component of human skin dermoepidermal junction.

J. Couchman, J. Fine, 1988, The Journal of investigative dermatology.

Gastric outlet obstruction and epidermolysis bullosa.

J. Wang-Rodriguez, D. Piacquadio, L. Eichenfield, 1997, Journal of the American Academy of Dermatology.

Intracytoplasmic retention of type VII collagen and dominant dystrophic epidermolysis bullosa: reversal of defect following cessation of or marked improvement in disease activity.

I. Leigh, J. T. Wright, R. Briggaman, 1993, The Journal of investigative dermatology.

Basic Fibroblast Growth Factor: A Missing Link between Collagen VII, Increased Collagenase, and Squamous Cell Carcinoma in Recessive Dystrophic Epidermolysis Bullosa

J. Folkman, J. Arbiser, A. Paller, 1998, Molecular medicine.

Three new cases of transient bullous dermolysis of the newborn.

J. Fine, M. Levy, S. G. Hanson, 1999, Journal of the American Academy of Dermatology.

Intraepidermal type VII collagen. Evidence for abnormal intracytoplasmic processing of a major basement membrane protein in rare patients with dominant and possibly localized recessive forms of dystrophic epidermolysis bullosa.

I. Leigh, Y. Horiguchi, J. Fine, 1990, Journal of the American Academy of Dermatology.

The carboxyl-terminal domain of type VII collagen is present at the basement membrane in recessive dystrophic epidermolysis bullosa.

R. Briggaman, J. Fine, W. Gammon, 1989, The Journal of investigative dermatology.

University of Groningen Management of cutaneous squamous cell carcinoma in patients with epidermolysis bullosa

J. McGrath, D. Murrell, A. Diem, 2020 .

Dystrophic epidermolysis bullosa inversa: report of two cases with further correlation between electron microscopic and immunofluorescence studies.

J. Fine, A. Lin, L. Smith, 1995, Journal of the American Academy of Dermatology.

Normal molecular weight of type VII collagen produced by recessive dystrophic epidermolysis bullosa keratinocytes.

J. Fine, E. O'Keefe, W. Gammon, 1993, The Journal of investigative dermatology.

Type VII collagen and 19-DEJ-1 antigen. Comparison of expression in inversa and generalized variants of recessive dystrophic epidermolysis bullosa.

J. Fine, L. Johnson, T. Wright, 1990, Archives of dermatology.

Prenatal exclusion of pyloric atresia-junctional epidermolysis bullosa syndrome.

H. Shimizu, T. Nishikawa, J. Fine, 1994, Journal of the American Academy of Dermatology.

Ultrastructural and immunohistochemical characterization of basal cells in three-dimensional culture models of the skin

K. Toda, N. Isshiki, I. Leigh, 2004, Archives of Dermatological Research.

Development of verrucous plaques and gross hematuria in advanced cutaneous T-cell lymphoma.

S. Tyring, J. Fine, P. Lee, 1988, Archives of dermatology.

Development of neuroendocrine (Merkel cell) carcinoma mixed with squamous cell carcinoma in erythema ab igne.

S. Tyring, J. Fine, Patricia C. Lee, 1988, Archives of dermatology.

Adult scalded skin syndrome fatally complicated by mixed gram-negative sepsis and cellulitis.

J. Fine, T. Harrist, A. Bradley, 1981, Cutis.

Resistance to Narrowband Ultraviolet B Therapy Over Varicose Veins in Two Cases of Generalized Vitiligo

Z. Holcomb, J. Powers, J. Fine, 2017 .

Epidermolysis Bullosa. Clinical, Epidemiologic, and Laboratory Advances and the Findings of the National Epidermolysis Bullosa Registry

J. Fine, 2000 .

Immunoelectron microscopy of skin basement membrane zone antigens: a pre-embedding method using 1-nm immunogold with silver enhancement.

H. Shimizu, J. McGrath, R. Eady, 1994, Acta dermato-venereologica.

Fibroblast-derived dermal matrix drives development of aggressive cutaneous squamous cell carcinoma in patients with recessive dystrophic epidermolysis bullosa.

J. McGrath, I. Leigh, F. Hogg, 2012, Cancer research.

Congenital pyloric atresia in a newborn with extensive aplasia cutis congenita and epidermolysis bullosa simplex

J. Uitto, L. Pulkkinen, D. Morrell, 2000, The British journal of dermatology.

Epidemiology of Inherited Epidermolysis Bullosa Based on Incidence and Prevalence Estimates From the National Epidermolysis Bullosa Registry.

J. Fine, Jo-David Fine, 2016, JAMA dermatology.

Sequence of reconstitution of seven basement-membrane components following split-thickness wound induction in primate skin.

A. Goodman, J. Fine, D. A. Redmar, 1987, Archives of dermatology.

The use of monoclonal antibodies in skin basement membrane research.

J. Fine, 1984, Collagen and related research.

Junctional epidermolysis bullosa with pyloric stenosis

D. Morrell, J. Fine, 2001, Pediatric dermatology.

Loss of kindlin-1, a human homolog of the Caenorhabditis elegans actin-extracellular-matrix linker protein UNC-112, causes Kindler syndrome.

H. Feiler, E. Fuchs, A. Prescott, 2003, American journal of human genetics.

Monoclonal antibodies in dermatologic research. Studies with a unique cell-surface antigen defined specifically for keratinocytes by a monoclonal antibody.

S. Katz, J. Fine, J. Stanley, 1985, The American Journal of dermatopathology.

Autoantibodies to extracellular collagen matrix components in epidermolysis bullosa and other bullous diseases

S. Gay, J. Fine, J. Storer, 2004, Archives of Dermatological Research.

Idiopathic Localized Unilateral Hyperhidrosis in a Child

F. Ghali, J. Fine, Fred E. Ghali, 2000, Pediatric dermatology.

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.

EB simplex superficialis resulting from a mutation in the type VII collagen gene.

J. Ott, T. Gilliam, Jianjun Liu, 2002, The Journal of investigative dermatology.

Life with Epidermolysis Bullosa (EB)

J. Fine, H. Hintner, 2009 .

Kindler syndrome and epidermolysis bullosa simplex.

J. Fine, N. Esterly, J. Prendiville, 1990, Journal of the American Academy of Dermatology.

Epidermolysis Bullosa Registries and the Epidemiology of Epidermolysis Bullosa (EB)

J. Fine, 2015 .

Malignant melanoma and epidermolysis bullosa simplex.

J. Fine, 2013, JAMA dermatology.

Cumulative life course impairment by epidermolysis bullosa.

J. Fine, 2013, Current problems in dermatology.

Childhood Epidermolysis Bullosa Acquisita: Detection in a 5-Year-Old Girl

J. Fine, N. Esterly, R. Rubenstein, 1987 .

Immunological and molecular approaches to the study of basement membrane proteoglycan diversity.

D. Abrahamson, J. Couchman, K. McCarthy, 1990, Biochemical Society Transactions.

Loeffler's syndrome?

J. Fine, 1979, Archives of dermatology.

The skin basement membrane zone.

J. Fine, 1987, Advances in dermatology.

Extensive variant of cutaneous amyloidosis: report of a case with electron-microscopic and immunohistochemical studies of the basement membrane zone at sites of amyloid production.

K. Danno, I. Leigh, Y. Horiguchi, 1992, Dermatology.

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

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

Inherited epidermolysis bullosa

J. Fine, 2010, Orphanet journal of rare diseases.

The risk of cardiomyopathy in inherited epidermolysis bullosa

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

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

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

Dystrophic epidermolysis bullosa. A new variant characterized by progressive symmetrical centripetal involvement with scarring.

S. Gay, J. Fine, L. S. Osment, 1985, 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.

Tetracycline and epidermolysis bullosa simplex: a double‐blind, placebo‐controlled, crossover randomized clinical trial

J. Fine, M. Weiner, A. Stein, 2004, British Journal of Dermatology.

Mosaic expression of uncein, linear IgA bullous dermatosis antigen and 180‐kDa bullous pemphigoid antigen in generalized atrophic benign epidermolysis bullosa

M. Jonkman, J. Fine, H. Pas, 1998, The British journal 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.

Human skin basement membrane‐associated heparan sulphate proteoglycan: distinctive differences in ultrastructural localization as a function of developmental age

J. Couchman, Y. Horiguchi, J. Fine, 1991, The British journal of dermatology.

A mouse model of generalized non-Herlitz junctional epidermolysis bullosa.

J. Sundberg, J. Bubier, D. Roopenian, 2010, The Journal of investigative dermatology.

Epidermolysis bullosa

C. Has, J. Mellerio, L. Bruckner-Tuderman, 2020, Nature Reviews Disease Primers.

Prevalence of autoantibodies to bullous pemphigoid antigens within the normal population.

J. Fine, 2010, Archives of dermatology.

Inherited epidermolysis bullosa

J. Fine, 2010, Orphanet journal of rare diseases.

Childhood epidermolysis bullosa acquisita. Detection in a 5-year-old girl.

J. Fine, N. Esterly, R. Rubenstein, 1987, Archives of dermatology.

UNCEIN MAY BE A POTENTIAL TARGET FOR SULFUR MUSTARD ALKYLATION

N. Monteiro-Riviere, J. Fine, Zili Zhang, 1998 .

Altered skin basement membrane antigenicity in epidermolysis bullosa.

J. Fine, 1987, Current problems in dermatology.