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Journal of Cutaneous Pathology
|
April 1, 1992
Epidermolysis bullosa complicated by squamous cell carcinoma: report of 10 cases
J A McGrath, O M Schofield, B J Mayou, et al.
British Medical Journal
|
March 22, 1975
Plasma immunoreactive melanotrophic hormones in patients on maintenance haemodialysis
J J Gilkes, R A Eady, L H Rees, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology
|
August 1, 2007
Prenatal diagnosis and management strategies in a family with a rare type of congenital ichthyosis
S V Phadnis, D R Griffin, R A Eady, et al.
The British Journal of Dermatology
|
December 1, 1994
Filaggrin expression in epidermolytic ichthyosis (epidermolytic hyperkeratosis)
A Ishida-Yamamoto, R A Eady, R A Underwood, et al.
The Journal of Investigative Dermatology
|
November 6, 1998
Severe palmo-plantar hyperkeratosis in Dowling-Meara epidermolysis bullosa simplex caused by a mutation in the keratin 14 gene (KRT14)
C S Shemanko, J E Mellerio, M J Tidman, et al.
The British Journal of Dermatology
|
September 5, 2001
New mutations in keratin 1 that cause bullous congenital ichthyosiform erythroderma and keratin 2e that cause ichthyosis bullosa of Siemens
N V Whittock, G H Ashton, W A Griffiths, et al.
Clinical and Experimental Dermatology
|
September 1, 1977
A new method for recovery of exudates from normal and inflamed human skin
A K Black, M W Greaves, C N Hensby, et al.
The Journal of Investigative Dermatology
|
April 1, 1995
Altered laminin 5 expression due to mutations in the gene encoding the beta 3 chain (LAMB3) in generalized atrophic benign epidermolysis bullosa
J A McGrath, L Pulkkinen, A M Christiano, et al.
Human Molecular Genetics
|
September 1, 1994
A novel homozygous point mutation in the collagen VII gene (COL7A1) in two cousins with recessive dystrophic epidermolysis bullosa
M G Dunnill, A J Richards, G Milana, et al.
The Journal of Cell Biology
|
March 1, 1996
Gene targeting at the mouse cytokeratin 10 locus: severe skin fragility and changes of cytokeratin expression in the epidermis
R M Porter, S Leitgeb, D W Melton, et al.
Page
of 21
Search research articles
Search
Showing results (121-130 of 206) with videos related to
Sort By:
Page
of 21
Journal of Cutaneous Pathology
|
April 1, 1992
Epidermolysis bullosa complicated by squamous cell carcinoma: report of 10 cases
J A McGrath, O M Schofield, B J Mayou, et al.
British Medical Journal
|
March 22, 1975
Plasma immunoreactive melanotrophic hormones in patients on maintenance haemodialysis
J J Gilkes, R A Eady, L H Rees, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology
|
August 1, 2007
Prenatal diagnosis and management strategies in a family with a rare type of congenital ichthyosis
S V Phadnis, D R Griffin, R A Eady, et al.
The British Journal of Dermatology
|
December 1, 1994
Filaggrin expression in epidermolytic ichthyosis (epidermolytic hyperkeratosis)
A Ishida-Yamamoto, R A Eady, R A Underwood, et al.
The Journal of Investigative Dermatology
|
November 6, 1998
Severe palmo-plantar hyperkeratosis in Dowling-Meara epidermolysis bullosa simplex caused by a mutation in the keratin 14 gene (KRT14)
C S Shemanko, J E Mellerio, M J Tidman, et al.
The British Journal of Dermatology
|
September 5, 2001
New mutations in keratin 1 that cause bullous congenital ichthyosiform erythroderma and keratin 2e that cause ichthyosis bullosa of Siemens
N V Whittock, G H Ashton, W A Griffiths, et al.
Clinical and Experimental Dermatology
|
September 1, 1977
A new method for recovery of exudates from normal and inflamed human skin
A K Black, M W Greaves, C N Hensby, et al.
The Journal of Investigative Dermatology
|
April 1, 1995
Altered laminin 5 expression due to mutations in the gene encoding the beta 3 chain (LAMB3) in generalized atrophic benign epidermolysis bullosa
J A McGrath, L Pulkkinen, A M Christiano, et al.
Human Molecular Genetics
|
September 1, 1994
A novel homozygous point mutation in the collagen VII gene (COL7A1) in two cousins with recessive dystrophic epidermolysis bullosa
M G Dunnill, A J Richards, G Milana, et al.
The Journal of Cell Biology
|
March 1, 1996
Gene targeting at the mouse cytokeratin 10 locus: severe skin fragility and changes of cytokeratin expression in the epidermis
R M Porter, S Leitgeb, D W Melton, et al.
Page
of 21