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The British Journal of Dermatology
|
May 18, 2013
Clinical experience and psychometric properties of the Children's Dermatology Life Quality Index (CDLQI), 1995-2012
M S Salek, S Jung, L A Brincat-Ruffini, et al.
Respiratory Medicine
|
January 1, 1995
Late pulmonary sequela following burns: persistence of hyperprocalcitonemia using a 1-57 amino acid N-terminal flanking peptide assay
E S Nylen, J Jeng, M H Jordan, et al.
Molecular and Cellular Biology
|
January 12, 2001
Inactivation of DNA mismatch repair by increased expression of yeast MLH1
P V Shcherbakova, M C Hall, M S Lewis, et al.
The Anatomical Record
|
May 1, 1993
Hypercalcitonemia in inhalation burn injury: a response of the pulmonary neuroendocrine cell?
K L Becker, W J O'Neil, R H Snider, et al.
Hearing Research
|
December 4, 2016
Audiologic characteristics in a sample of recently-separated military Veterans: The Noise Outcomes in Servicemembers Epidemiology Study (NOISE Study)
J S Gordon, S E Griest, E J Thielman, et al.
Biochemistry
|
December 7, 1993
Structure/function studies of HIV-1(1) reverse transcriptase: dimerization-defective mutant L289K
R Goel, W A Beard, A Kumar, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology
|
August 16, 2002
An international evaluation of CODOX-M and CODOX-M alternating with IVAC in adult Burkitt's lymphoma: results of United Kingdom Lymphoma Group LY06 study
G M Mead, M R Sydes, J Walewski, et al.
Clinical and Laboratory Haematology
|
December 21, 2000
A capillary whole blood method for measuring the INR
E J Bamford, R H Bowen, J P Broad, et al.
The British Journal of Dermatology
|
January 1, 1997
Long-term efficacy and safety of cyclosporin in severe adult atopic dermatitis
J Berth-Jones, R A Graham-Brown, R Marks, et al.
Human Molecular Genetics
|
May 23, 2003
Genetic and functional analyses of FH mutations in multiple cutaneous and uterine leiomyomatosis, hereditary leiomyomatosis and renal cancer, and fumarate hydratase deficiency
N A Alam, A J Rowan, N C Wortham, et al.
Page
of 13
Search research articles
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Showing results (121-130 of 130) with videos related to
Sort By:
Page
of 13
You have reached the last page of results.
This site can display upto 130 results.
The British Journal of Dermatology
|
May 18, 2013
Clinical experience and psychometric properties of the Children's Dermatology Life Quality Index (CDLQI), 1995-2012
M S Salek, S Jung, L A Brincat-Ruffini, et al.
Respiratory Medicine
|
January 1, 1995
Late pulmonary sequela following burns: persistence of hyperprocalcitonemia using a 1-57 amino acid N-terminal flanking peptide assay
E S Nylen, J Jeng, M H Jordan, et al.
Molecular and Cellular Biology
|
January 12, 2001
Inactivation of DNA mismatch repair by increased expression of yeast MLH1
P V Shcherbakova, M C Hall, M S Lewis, et al.
The Anatomical Record
|
May 1, 1993
Hypercalcitonemia in inhalation burn injury: a response of the pulmonary neuroendocrine cell?
K L Becker, W J O'Neil, R H Snider, et al.
Hearing Research
|
December 4, 2016
Audiologic characteristics in a sample of recently-separated military Veterans: The Noise Outcomes in Servicemembers Epidemiology Study (NOISE Study)
J S Gordon, S E Griest, E J Thielman, et al.
Biochemistry
|
December 7, 1993
Structure/function studies of HIV-1(1) reverse transcriptase: dimerization-defective mutant L289K
R Goel, W A Beard, A Kumar, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology
|
August 16, 2002
An international evaluation of CODOX-M and CODOX-M alternating with IVAC in adult Burkitt's lymphoma: results of United Kingdom Lymphoma Group LY06 study
G M Mead, M R Sydes, J Walewski, et al.
Clinical and Laboratory Haematology
|
December 21, 2000
A capillary whole blood method for measuring the INR
E J Bamford, R H Bowen, J P Broad, et al.
The British Journal of Dermatology
|
January 1, 1997
Long-term efficacy and safety of cyclosporin in severe adult atopic dermatitis
J Berth-Jones, R A Graham-Brown, R Marks, et al.
Human Molecular Genetics
|
May 23, 2003
Genetic and functional analyses of FH mutations in multiple cutaneous and uterine leiomyomatosis, hereditary leiomyomatosis and renal cancer, and fumarate hydratase deficiency
N A Alam, A J Rowan, N C Wortham, et al.
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of 13