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The British Journal of Dermatology
|
July 4, 2018
Atopic dermatitis: the skin barrier and beyond
T Tsakok, R Woolf, C H Smith, et al.
European Journal of Pediatrics
|
March 21, 1998
Pericardial effusion in glycanosis CDG type I (MIM 212 065): an inflammatory endoplasmic reticulum overload response?
K Heyne, E Mayatepek, F Walther, et al.
European Journal of Medical Research
|
December 17, 2005
Alpha-1-antitrypsin deficiency in children: liver disease is not reflected by low serum levels of alpha-1-antitrypsin - a study on 48 pediatric patients
Thomas Lang, M Mühlbauer, M Strobelt, et al.
Human Genetics
|
January 1, 1984
Transferrin subtypes and variants in Germany; further evidence for a Tf null allele
S Weidinger, H Cleve, F Schwarzfischer, et al.
European Journal of Pediatrics
|
November 1, 1994
Hypothyroidism phenocopy in glycanosis CDG (carbohydrate-deficient glycoprotein syndrome)
K Heyne, W Marg, F Walther, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
June 30, 1987
Agarose gel isoelectrofocusing of UDP-galactose pyrophosphorylase and galactose-1-phosphate uridyltransferase. Developmental aspect of UDP-galactose pyrophosphorylase
Y S Shin, H P Niedermeier, W Endres, et al.
Psychoneuroendocrinology
|
November 13, 2012
Psychoendocrine and psychoneuroimmunological mechanisms in the comorbidity of atopic eczema and attention deficit/hyperactivity disorder
A Buske-Kirschbaum, J Schmitt, F Plessow, et al.
World Neurosurgery
|
March 21, 2024
Early Intravenous Magnesium Sulfate and Its Impact on Cerebral Vasospasm as well as Delayed Cerebral Ischemia in Aneurysmal Subarachnoid Hemorrhage: A Retrospective Matched Case-Control Analysis
Julian Feulner, Cornelia S Weidinger, Arnd Dörfler, et al.
Human Genetics
|
May 1, 1986
Extended polymorphism of the human esterase D isozyme system: description of a "new" allele EsD*11
J Henke, H Schweitzer, W Bär, et al.
Human Genetics
|
March 1, 1992
PGD Port Elizabeth: a new variant found in South Africa
T Schlaphoff, S Weidinger, W Petersen, et al.
Page
of 13
Search research articles
Search
Showing results (51-60 of 129) with videos related to
Sort By:
Page
of 13
The British Journal of Dermatology
|
July 4, 2018
Atopic dermatitis: the skin barrier and beyond
T Tsakok, R Woolf, C H Smith, et al.
European Journal of Pediatrics
|
March 21, 1998
Pericardial effusion in glycanosis CDG type I (MIM 212 065): an inflammatory endoplasmic reticulum overload response?
K Heyne, E Mayatepek, F Walther, et al.
European Journal of Medical Research
|
December 17, 2005
Alpha-1-antitrypsin deficiency in children: liver disease is not reflected by low serum levels of alpha-1-antitrypsin - a study on 48 pediatric patients
Thomas Lang, M Mühlbauer, M Strobelt, et al.
Human Genetics
|
January 1, 1984
Transferrin subtypes and variants in Germany; further evidence for a Tf null allele
S Weidinger, H Cleve, F Schwarzfischer, et al.
European Journal of Pediatrics
|
November 1, 1994
Hypothyroidism phenocopy in glycanosis CDG (carbohydrate-deficient glycoprotein syndrome)
K Heyne, W Marg, F Walther, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
June 30, 1987
Agarose gel isoelectrofocusing of UDP-galactose pyrophosphorylase and galactose-1-phosphate uridyltransferase. Developmental aspect of UDP-galactose pyrophosphorylase
Y S Shin, H P Niedermeier, W Endres, et al.
Psychoneuroendocrinology
|
November 13, 2012
Psychoendocrine and psychoneuroimmunological mechanisms in the comorbidity of atopic eczema and attention deficit/hyperactivity disorder
A Buske-Kirschbaum, J Schmitt, F Plessow, et al.
World Neurosurgery
|
March 21, 2024
Early Intravenous Magnesium Sulfate and Its Impact on Cerebral Vasospasm as well as Delayed Cerebral Ischemia in Aneurysmal Subarachnoid Hemorrhage: A Retrospective Matched Case-Control Analysis
Julian Feulner, Cornelia S Weidinger, Arnd Dörfler, et al.
Human Genetics
|
May 1, 1986
Extended polymorphism of the human esterase D isozyme system: description of a "new" allele EsD*11
J Henke, H Schweitzer, W Bär, et al.
Human Genetics
|
March 1, 1992
PGD Port Elizabeth: a new variant found in South Africa
T Schlaphoff, S Weidinger, W Petersen, et al.
Page
of 13