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Acta Endocrinologica
|
June 1, 1985
Prolactinoma of the pituitary containing amyloid
A Paetau, S Partanen, P Mustajoki, et al.
Molecular Medicine (Cambridge, Mass.)
|
October 31, 2000
Acute intermittent porphyria: expression of mutant and wild-type porphobilinogen deaminase in COS-1 cells
S Mustajoki, M Laine, M Lahtela, et al.
Human Genetics
|
July 8, 1998
Three splicing defects, an insertion, and two missense mutations responsible for acute intermittent porphyria
S Mustajoki, H Pihlaja, H Ahola, et al.
International Journal of Obesity and Related Metabolic Disorders : Journal of the International Association for the Study of Obesity
|
June 1, 1997
Novel polymorphism of the human ob gene promoter in lean and morbidly obese subjects
L Oksanen, K Kainulainen, M Heiman, et al.
European Journal of Clinical Investigation
|
June 1, 1992
Sustained high plasma 5-aminolaevulinic acid concentration in a volunteer: no porphyric symptoms
P Mustajoki, K Timonen, A Gorchein, et al.
Diabetes, Obesity & Metabolism
|
April 2, 2004
Changes in sex hormone-binding globulin and testosterone during weight loss and weight maintenance in abdominally obese men with the metabolic syndrome
L Niskanen, D E Laaksonen, K Punnonen, et al.
Clinical Genetics
|
November 1, 1987
Homozygous variegate porphyria. A severe skin disease of infancy
P Mustajoki, R Tenhunen, K M Niemi, et al.
BMJ (Clinical Research Ed.)
|
March 24, 2000
Immediate and long term effects of weight reduction in obese people with asthma: randomised controlled study
B Stenius-Aarniala, T Poussa, J Kvarnström, et al.
International Journal of Obesity and Related Metabolic Disorders : Journal of the International Association for the Study of Obesity
|
December 1, 1996
Polymorphism of the beta 3-adrenergic receptor gene in morbid obesity
L Oksanen, P Mustajoki, J Kaprio, et al.
The Journal of Investigative Dermatology
|
February 1, 1996
Four novel mutations in the ferrochelatase gene among erythropoietic protoporphyria patients
M Henriksson, K Timonen, P Mustajoki, et al.
Page
of 11
Search research articles
Search
Showing results (91-100 of 109) with videos related to
Sort By:
Page
of 11
Acta Endocrinologica
|
June 1, 1985
Prolactinoma of the pituitary containing amyloid
A Paetau, S Partanen, P Mustajoki, et al.
Molecular Medicine (Cambridge, Mass.)
|
October 31, 2000
Acute intermittent porphyria: expression of mutant and wild-type porphobilinogen deaminase in COS-1 cells
S Mustajoki, M Laine, M Lahtela, et al.
Human Genetics
|
July 8, 1998
Three splicing defects, an insertion, and two missense mutations responsible for acute intermittent porphyria
S Mustajoki, H Pihlaja, H Ahola, et al.
International Journal of Obesity and Related Metabolic Disorders : Journal of the International Association for the Study of Obesity
|
June 1, 1997
Novel polymorphism of the human ob gene promoter in lean and morbidly obese subjects
L Oksanen, K Kainulainen, M Heiman, et al.
European Journal of Clinical Investigation
|
June 1, 1992
Sustained high plasma 5-aminolaevulinic acid concentration in a volunteer: no porphyric symptoms
P Mustajoki, K Timonen, A Gorchein, et al.
Diabetes, Obesity & Metabolism
|
April 2, 2004
Changes in sex hormone-binding globulin and testosterone during weight loss and weight maintenance in abdominally obese men with the metabolic syndrome
L Niskanen, D E Laaksonen, K Punnonen, et al.
Clinical Genetics
|
November 1, 1987
Homozygous variegate porphyria. A severe skin disease of infancy
P Mustajoki, R Tenhunen, K M Niemi, et al.
BMJ (Clinical Research Ed.)
|
March 24, 2000
Immediate and long term effects of weight reduction in obese people with asthma: randomised controlled study
B Stenius-Aarniala, T Poussa, J Kvarnström, et al.
International Journal of Obesity and Related Metabolic Disorders : Journal of the International Association for the Study of Obesity
|
December 1, 1996
Polymorphism of the beta 3-adrenergic receptor gene in morbid obesity
L Oksanen, P Mustajoki, J Kaprio, et al.
The Journal of Investigative Dermatology
|
February 1, 1996
Four novel mutations in the ferrochelatase gene among erythropoietic protoporphyria patients
M Henriksson, K Timonen, P Mustajoki, et al.
Page
of 11