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R A Eady

Showing results (131-140 of 206) with videos related to

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The Journal of Histochemistry and Cytochemistry : Official Journal of the Histochemistry Society|February 1, 1996
Immunoelectron microscopic analysis of cornified cell envelope formation in normal and psoriatic epidermisA Ishida-Yamamoto, R A Eady, F M Watt, et al.
Journal of Medical Genetics|June 1, 1992
Linkage of autosomal dominant dystrophic epidermolysis bullosa in three British families to the marker D3S2 close to the COL7A1 locusL al-Imara, A J Richards, R A Eady, et al.
The Journal of Investigative Dermatology|August 22, 2000
Genomic amplification of the human plakophilin 1 gene and detection of a new mutation in ectodermal dysplasia/skin fragility syndromeN V Whittock, M Haftek, N Angoulvant, et al.
Journal of the American Academy of Dermatology|December 1, 1990
GB3 monoclonal antibody for the diagnosis of junctional epidermolysis bullosa: results of a multicenter studyO M Schofield, J D Fine, P Verrando, et al.
The Journal of Investigative Dermatology|November 1, 1993
Nicein (BM-600) in junctional epidermolysis bullosa: polyclonal antibodies provide new clues for pathogenic roleP Verrando, O Schofield, A Ishida-Yamamoto, et al.
The British Journal of Dermatology|March 17, 2001
Alpha 6 beta 4 integrin abnormalities in junctional epidermolysis bullosa with pyloric atresiaG H Ashton, P Sorelli, J E Mellerio, et al.
The Journal of Investigative Dermatology|July 1, 1992
Selective involvement of keratins K1 and K10 in the cytoskeletal abnormality of epidermolytic hyperkeratosis (bullous congenital ichthyosiform erythroderma)A Ishida-Yamamoto, J A McGrath, M R Judge, et al.
The British Journal of Dermatology|May 1, 1992
Epidermolysis bullosa simplex (Dowling-Meara). A clinicopathological reviewJ A McGrath, A Ishida-Yamamoto, M J Tidman, et al.
Journal of Medical Genetics|February 1, 1986
Prenatal diagnosis of bullous ichthyosiform erythroderma: detection of tonofilament clumps in fetal epidermal and amniotic fluid cellsR A Eady, D B Gunner, L D Carbone, et al.
The Journal of Investigative Dermatology|December 1, 1991
Epidermolysis bullosa simplex (Dowling-Meara type) is a genetic disease characterized by an abnormal keratin-filament network involving keratins K5 and K14A Ishida-Yamamoto, J A McGrath, S J Chapman, et al.
Pageof 21

Showing results (131-140 of 206) with videos related to

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Pageof 21
The Journal of Histochemistry and Cytochemistry : Official Journal of the Histochemistry Society|February 1, 1996
Immunoelectron microscopic analysis of cornified cell envelope formation in normal and psoriatic epidermisA Ishida-Yamamoto, R A Eady, F M Watt, et al.
Journal of Medical Genetics|June 1, 1992
Linkage of autosomal dominant dystrophic epidermolysis bullosa in three British families to the marker D3S2 close to the COL7A1 locusL al-Imara, A J Richards, R A Eady, et al.
The Journal of Investigative Dermatology|August 22, 2000
Genomic amplification of the human plakophilin 1 gene and detection of a new mutation in ectodermal dysplasia/skin fragility syndromeN V Whittock, M Haftek, N Angoulvant, et al.
Journal of the American Academy of Dermatology|December 1, 1990
GB3 monoclonal antibody for the diagnosis of junctional epidermolysis bullosa: results of a multicenter studyO M Schofield, J D Fine, P Verrando, et al.
The Journal of Investigative Dermatology|November 1, 1993
Nicein (BM-600) in junctional epidermolysis bullosa: polyclonal antibodies provide new clues for pathogenic roleP Verrando, O Schofield, A Ishida-Yamamoto, et al.
The British Journal of Dermatology|March 17, 2001
Alpha 6 beta 4 integrin abnormalities in junctional epidermolysis bullosa with pyloric atresiaG H Ashton, P Sorelli, J E Mellerio, et al.
The Journal of Investigative Dermatology|July 1, 1992
Selective involvement of keratins K1 and K10 in the cytoskeletal abnormality of epidermolytic hyperkeratosis (bullous congenital ichthyosiform erythroderma)A Ishida-Yamamoto, J A McGrath, M R Judge, et al.
The British Journal of Dermatology|May 1, 1992
Epidermolysis bullosa simplex (Dowling-Meara). A clinicopathological reviewJ A McGrath, A Ishida-Yamamoto, M J Tidman, et al.
Journal of Medical Genetics|February 1, 1986
Prenatal diagnosis of bullous ichthyosiform erythroderma: detection of tonofilament clumps in fetal epidermal and amniotic fluid cellsR A Eady, D B Gunner, L D Carbone, et al.
The Journal of Investigative Dermatology|December 1, 1991
Epidermolysis bullosa simplex (Dowling-Meara type) is a genetic disease characterized by an abnormal keratin-filament network involving keratins K5 and K14A Ishida-Yamamoto, J A McGrath, S J Chapman, et al.
Pageof 21