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Archives of Disease in Childhood. Fetal and Neonatal Edition
|
May 18, 1999
Blood concentrations of pancreatitis associated protein in neonates: relevance to neonatal screening for cystic fibrosis
J Sarles, S Barthellemy, C Férec, et al.
Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie
|
September 21, 2025
Amphiregulin reflects brain metastasis progression and leads to PD-L1 expression in non-small cell lung cancer cells
Dimitri Leite Ferreira, Tiphaine Biojout, Céline Bazille, et al.
The Journal of Small Animal Practice
|
July 1, 2025
Understanding the rationale for metronidazole use in dogs and cats
J Ng, N Steffensen, I Battersby, et al.
Skin Health and Disease
|
December 3, 2024
T-cell-related skin inflammatory flareups with Th1 polarity in a patient with pseudoxanthoma elasticum
Samuel Rocour, Emeline Vinatier, Céline Fassot, et al.
Annales De Biologie Clinique
|
August 16, 2024
[Acquired hemophilia A and emicizumab for the treatment of bleeding: two case report and a literature review]
Amélie Launois, Isabelle Martin-Toutain, Floriane Devaux, et al.
Antibiotics (Basel, Switzerland)
|
April 3, 2021
Towards a Better and Harmonized Education in Antimicrobial Stewardship in European Veterinary Curricula
Carmen Espinosa-Gongora, Lisbeth Rem Jessen, Oliver James Dyar, et al.
Journal of Applied Physiology (Bethesda, Md. : 1985)
|
December 15, 2015
Acute effects of changes to the gravitational vector on the eye
Allison P Anderson, Jacob G Swan, Scott D Phillips, et al.
American Journal of Medical Genetics. Part A
|
December 11, 2012
Cerebellar and posterior fossa malformations in patients with autism-associated chromosome 22q13 terminal deletion
Kimberly A Aldinger, Jillene Kogan, Virginia Kimonis, et al.
Pigment Cell & Melanoma Research
|
October 15, 2013
High-resolution array-CGH in patients with oculocutaneous albinism identifies new deletions of the TYR, OCA2, and SLC45A2 genes and a complex rearrangement of the OCA2 gene
Fanny Morice-Picard, Eulalie Lasseaux, Dorothée Cailley, et al.
Gene
|
October 16, 2012
Validation of high-resolution DNA melting analysis for mutation scanning of the CDKL5 gene: identification of novel mutations
Laure Raymond, Bertrand Diebold, Céline Leroux, et al.
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Search research articles
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Showing results (631-640 of 885) with videos related to
Sort By:
Page
of 89
Archives of Disease in Childhood. Fetal and Neonatal Edition
|
May 18, 1999
Blood concentrations of pancreatitis associated protein in neonates: relevance to neonatal screening for cystic fibrosis
J Sarles, S Barthellemy, C Férec, et al.
Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie
|
September 21, 2025
Amphiregulin reflects brain metastasis progression and leads to PD-L1 expression in non-small cell lung cancer cells
Dimitri Leite Ferreira, Tiphaine Biojout, Céline Bazille, et al.
The Journal of Small Animal Practice
|
July 1, 2025
Understanding the rationale for metronidazole use in dogs and cats
J Ng, N Steffensen, I Battersby, et al.
Skin Health and Disease
|
December 3, 2024
T-cell-related skin inflammatory flareups with Th1 polarity in a patient with pseudoxanthoma elasticum
Samuel Rocour, Emeline Vinatier, Céline Fassot, et al.
Annales De Biologie Clinique
|
August 16, 2024
[Acquired hemophilia A and emicizumab for the treatment of bleeding: two case report and a literature review]
Amélie Launois, Isabelle Martin-Toutain, Floriane Devaux, et al.
Antibiotics (Basel, Switzerland)
|
April 3, 2021
Towards a Better and Harmonized Education in Antimicrobial Stewardship in European Veterinary Curricula
Carmen Espinosa-Gongora, Lisbeth Rem Jessen, Oliver James Dyar, et al.
Journal of Applied Physiology (Bethesda, Md. : 1985)
|
December 15, 2015
Acute effects of changes to the gravitational vector on the eye
Allison P Anderson, Jacob G Swan, Scott D Phillips, et al.
American Journal of Medical Genetics. Part A
|
December 11, 2012
Cerebellar and posterior fossa malformations in patients with autism-associated chromosome 22q13 terminal deletion
Kimberly A Aldinger, Jillene Kogan, Virginia Kimonis, et al.
Pigment Cell & Melanoma Research
|
October 15, 2013
High-resolution array-CGH in patients with oculocutaneous albinism identifies new deletions of the TYR, OCA2, and SLC45A2 genes and a complex rearrangement of the OCA2 gene
Fanny Morice-Picard, Eulalie Lasseaux, Dorothée Cailley, et al.
Gene
|
October 16, 2012
Validation of high-resolution DNA melting analysis for mutation scanning of the CDKL5 gene: identification of novel mutations
Laure Raymond, Bertrand Diebold, Céline Leroux, et al.
Page
of 89