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The Journal of Investigative Dermatology
|
January 29, 2000
Epidermolysis bullosa: novel and de novo premature termination codon and deletion mutations in the plectin gene predict late-onset muscular dystrophy
F Rouan, L Pulkkinen, G Meneguzzi, et al.
The Journal of Investigative Dermatology
|
November 6, 1998
The 97 kDa linear IgA bullous dermatosis antigen is not expressed in a patient with generalized atrophic benign epidermolysis bullosa with a novel homozygous G258X mutation in COL17A1
H Shimizu, Y Takizawa, L Pulkkinen, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation
|
June 30, 2000
Congenital focal segmental glomerulosclerosis associated with beta4 integrin mutation and epidermolysis bullosa
N Kambham, N Tanji, R L Seigle, et al.
European Journal of Endocrinology
|
February 27, 2008
Serum concentrations and expressions of serum amyloid A and leptin in adipose tissue are interrelated: the Genobin Study
T Lappalainen, M Kolehmainen, U Schwab, et al.
International Journal of Obesity (2005)
|
April 2, 2009
Genetic and environmental effects on body mass index during adolescence: a prospective study among Finnish twins
H-R Lajunen, J Kaprio, A Keski-Rahkonen, et al.
Genomics
|
November 15, 1994
A homozygous nonsense mutation in the beta 3 chain gene of laminin 5 (LAMB3) in Herlitz junctional epidermolysis bullosa
L Pulkkinen, A M Christiano, D Gerecke, et al.
Psychological Medicine
|
July 8, 2011
Prospective relationships of ADHD symptoms with developing substance use in a population-derived sample
E Sihvola, R J Rose, D M Dick, et al.
The Journal of Investigative Dermatology
|
March 7, 2001
Is screening of the candidate gene necessary in unrelated partners of members of families with Herlitz junctional epidermolysis bullosa?
A Klausegger, L Pulkkinen, G Pohla-Gubo, et al.
Journal of the American Academy of Dermatology
|
November 26, 1999
Epidermolysis bullosa simplex associated with muscular dystrophy: phenotype-genotype correlations and review of the literature
H Shimizu, Y Takizawa, L Pulkkinen, et al.
The Journal of Antimicrobial Chemotherapy
|
October 1, 1985
Trimethoprim resistance of Escherichia coli in outpatients in Finland after ten years' use of plain trimethoprim
P Huovinen, O V Renkonen, L Pulkkinen, et al.
Page
of 14
Search research articles
Search
Showing results (91-100 of 138) with videos related to
Sort By:
Page
of 14
The Journal of Investigative Dermatology
|
January 29, 2000
Epidermolysis bullosa: novel and de novo premature termination codon and deletion mutations in the plectin gene predict late-onset muscular dystrophy
F Rouan, L Pulkkinen, G Meneguzzi, et al.
The Journal of Investigative Dermatology
|
November 6, 1998
The 97 kDa linear IgA bullous dermatosis antigen is not expressed in a patient with generalized atrophic benign epidermolysis bullosa with a novel homozygous G258X mutation in COL17A1
H Shimizu, Y Takizawa, L Pulkkinen, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation
|
June 30, 2000
Congenital focal segmental glomerulosclerosis associated with beta4 integrin mutation and epidermolysis bullosa
N Kambham, N Tanji, R L Seigle, et al.
European Journal of Endocrinology
|
February 27, 2008
Serum concentrations and expressions of serum amyloid A and leptin in adipose tissue are interrelated: the Genobin Study
T Lappalainen, M Kolehmainen, U Schwab, et al.
International Journal of Obesity (2005)
|
April 2, 2009
Genetic and environmental effects on body mass index during adolescence: a prospective study among Finnish twins
H-R Lajunen, J Kaprio, A Keski-Rahkonen, et al.
Genomics
|
November 15, 1994
A homozygous nonsense mutation in the beta 3 chain gene of laminin 5 (LAMB3) in Herlitz junctional epidermolysis bullosa
L Pulkkinen, A M Christiano, D Gerecke, et al.
Psychological Medicine
|
July 8, 2011
Prospective relationships of ADHD symptoms with developing substance use in a population-derived sample
E Sihvola, R J Rose, D M Dick, et al.
The Journal of Investigative Dermatology
|
March 7, 2001
Is screening of the candidate gene necessary in unrelated partners of members of families with Herlitz junctional epidermolysis bullosa?
A Klausegger, L Pulkkinen, G Pohla-Gubo, et al.
Journal of the American Academy of Dermatology
|
November 26, 1999
Epidermolysis bullosa simplex associated with muscular dystrophy: phenotype-genotype correlations and review of the literature
H Shimizu, Y Takizawa, L Pulkkinen, et al.
The Journal of Antimicrobial Chemotherapy
|
October 1, 1985
Trimethoprim resistance of Escherichia coli in outpatients in Finland after ten years' use of plain trimethoprim
P Huovinen, O V Renkonen, L Pulkkinen, et al.
Page
of 14