Search research articles
Contact Us
Filters
Showing results (311-320 of 323) with videos related to
Page
of 33
Sort By:
International Journal of Molecular Sciences
|
June 27, 2024
Superelectrophilic Activation of Phosphacoumarins towards Weak Nucleophiles via Brønsted Acid Assisted Brønsted Acid Catalysis
Alena V Zalaltdinova, Yulia M Sadykova, Almir S Gazizov, et al.
Physical Review Letters
|
October 2, 2009
Molecular dissociative ionization and wave-packet dynamics studied using two-color XUV and IR pump-probe spectroscopy
F Kelkensberg, C Lefebvre, W Siu, et al.
Endocrine
|
December 16, 2014
Molecular analysis of PROP1, POU1F1, LHX3, and HESX1 in Turkish patients with combined pituitary hormone deficiency: a multicenter study
Firdevs Baş, Z Oya Uyguner, Feyza Darendeliler, et al.
The Turkish Journal of Pediatrics
|
December 24, 2008
Adult height in Turkish patients with Turner syndrome without growth hormone treatment
Abdullah Bereket, Serap Turan, Nursel Elçioğlu, et al.
Hormone Research in Paediatrics
|
March 30, 2012
The exon 3-deleted/full-length growth hormone receptor polymorphism and response to growth hormone therapy in growth hormone deficiency and Turner syndrome: a multicenter study
Firdevs Baş, Feyza Darendeliler, Zehra Aycan, et al.
Journal of Human Genetics
|
January 27, 2015
The phenotypic and molecular genetic spectrum of Alström syndrome in 44 Turkish kindreds and a literature review of Alström syndrome in Turkey
Ayşegül Ozantürk, Jan D Marshall, Gayle B Collin, et al.
Journal of Clinical Research in Pediatric Endocrinology
|
March 25, 2015
Current practice in diagnosis and treatment of growth hormone deficiency in childhood: a survey from Turkey
Şükran Poyrazoğlu, Teoman Akçay, İlknur Arslanoğlu, et al.
Journal of Human Genetics
|
October 10, 2014
The phenotypic and molecular genetic spectrum of Alström syndrome in 44 Turkish kindreds and a literature review of Alström syndrome in Turkey
Ayşegül Ozantürk, Jan D Marshall, Gayle B Collin, et al.
Journal of Clinical Research in Pediatric Endocrinology
|
November 7, 2018
Clinical and Laboratory Characteristics of Hyperprolactinemia in Children and Adolescents: National Survey
Erdal Eren, Ayça Törel Ergür, Şükriye Pınar İşgüven, et al.
Endocrine
|
July 17, 2024
17α Hydroxylase/17,20 lyase deficiency: clinical features and genetic insights from a large Turkey cohort
Zeynep Siklar, Emine Camtosun, Semih Bolu, et al.
Page
of 33
Search research articles
Search
Showing results (311-320 of 323) with videos related to
Sort By:
Page
of 33
International Journal of Molecular Sciences
|
June 27, 2024
Superelectrophilic Activation of Phosphacoumarins towards Weak Nucleophiles via Brønsted Acid Assisted Brønsted Acid Catalysis
Alena V Zalaltdinova, Yulia M Sadykova, Almir S Gazizov, et al.
Physical Review Letters
|
October 2, 2009
Molecular dissociative ionization and wave-packet dynamics studied using two-color XUV and IR pump-probe spectroscopy
F Kelkensberg, C Lefebvre, W Siu, et al.
Endocrine
|
December 16, 2014
Molecular analysis of PROP1, POU1F1, LHX3, and HESX1 in Turkish patients with combined pituitary hormone deficiency: a multicenter study
Firdevs Baş, Z Oya Uyguner, Feyza Darendeliler, et al.
The Turkish Journal of Pediatrics
|
December 24, 2008
Adult height in Turkish patients with Turner syndrome without growth hormone treatment
Abdullah Bereket, Serap Turan, Nursel Elçioğlu, et al.
Hormone Research in Paediatrics
|
March 30, 2012
The exon 3-deleted/full-length growth hormone receptor polymorphism and response to growth hormone therapy in growth hormone deficiency and Turner syndrome: a multicenter study
Firdevs Baş, Feyza Darendeliler, Zehra Aycan, et al.
Journal of Human Genetics
|
January 27, 2015
The phenotypic and molecular genetic spectrum of Alström syndrome in 44 Turkish kindreds and a literature review of Alström syndrome in Turkey
Ayşegül Ozantürk, Jan D Marshall, Gayle B Collin, et al.
Journal of Clinical Research in Pediatric Endocrinology
|
March 25, 2015
Current practice in diagnosis and treatment of growth hormone deficiency in childhood: a survey from Turkey
Şükran Poyrazoğlu, Teoman Akçay, İlknur Arslanoğlu, et al.
Journal of Human Genetics
|
October 10, 2014
The phenotypic and molecular genetic spectrum of Alström syndrome in 44 Turkish kindreds and a literature review of Alström syndrome in Turkey
Ayşegül Ozantürk, Jan D Marshall, Gayle B Collin, et al.
Journal of Clinical Research in Pediatric Endocrinology
|
November 7, 2018
Clinical and Laboratory Characteristics of Hyperprolactinemia in Children and Adolescents: National Survey
Erdal Eren, Ayça Törel Ergür, Şükriye Pınar İşgüven, et al.
Endocrine
|
July 17, 2024
17α Hydroxylase/17,20 lyase deficiency: clinical features and genetic insights from a large Turkey cohort
Zeynep Siklar, Emine Camtosun, Semih Bolu, et al.
Page
of 33