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Showing page 1 of results 1 - 10 of about 1000 matches for "mcmaster-a"

100% match
26 hit(s)
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A cyclin dependent kinase inhibitor 1B missense mutation (Pro69Leu) is associated with familial hypomagnesaemia, but not multiple endocrine neoplasia type 4 (MEN4) | SFEBES2019
Mark Stevenson; Eric Olinger; Huguette Debaix; Bruno Vogt; Olivier Devuyst; Rajesh Thakker
https://www.endocrine-abstracts.org/ea/0065/ea0065p140
Published: 2019-11-06

100% match
26 hit(s)
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A cyclin dependent kinase inhibitor 1B missense mutation (Pro69Leu) is associated with familial hypomagnesaemia, but not multiple endocrine neoplasia type 4 (MEN4) | SFEBES2019
Mark Stevenson; Eric Olinger; Huguette Debaix; Bruno Vogt; Olivier Devuyst; Rajesh Thakker
https://www.endocrine-abstracts.org/ea/0065/ea0065p140.htm
Published: 2019-11-06

97% match
18 hit(s)
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Health care professional & patient consultation - informed decision making | SFEBES2019
Antonia Brooke
https://www.endocrine-abstracts.org/ea/0065/ea0065ns1.2
Published: 2019-11-06

97% match
18 hit(s)
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Health care professional & patient consultation - informed decision making | SFEBES2019
Antonia Brooke
https://www.endocrine-abstracts.org/ea/0065/ea0065ns1.2.htm
Published: 2019-11-06

95% match
12 hit(s)
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Molecular Mechanisms of Idiopathic Ketotic Hypoglycemia in Children | ESPE2019
Tatiana Ivannikova; Natalya Milovanova; Ekaterina Zakharova; Dilyara Gubayeva; Maria Kareva; Maria Melikyan
http://abstracts.eurospe.org/hrp/0092/hrp0092P1-69
Published: 2019-08-22

95% match
12 hit(s)
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Molecular Mechanisms of Idiopathic Ketotic Hypoglycemia in Children | ESPE2019
Tatiana Ivannikova; Natalya Milovanova; Ekaterina Zakharova; Dilyara Gubayeva; Maria Kareva; Maria Melikyan
http://abstracts.eurospe.org/hrp/0092/hrp0092p1-69.html
Published: 2019-08-22

88% match
18 hit(s)
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Transcriptome Analysis of Novel Sertoli Cell Models to Highlight Potential Genes Involved in DSD Mechanism of Disease | ESPE2019
Daniel Rodríguez Gutiérrez; Patrick Sproll; Anna Biason-Lauber
http://abstracts.eurospe.org/hrp/0092/hrp0092FC10.5
Published: 2019-08-22

88% match
18 hit(s)
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Transcriptome Analysis of Novel Sertoli Cell Models to Highlight Potential Genes Involved in DSD Mechanism of Disease | ESPE2019
Daniel Rodríguez Gutiérrez; Patrick Sproll; Anna Biason-Lauber
http://abstracts.eurospe.org/hrp/0092/hrp0092fc10.5.html
Published: 2019-08-22

88% match
16 hit(s)
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Loss-Of-Function NNT Mutations Impair Antioxidants Mechanisms and Decreases Cortisol Secretion in Patients with Famililar Glucocorticoid Deficieny | ESPE2019
Bodoni Aline Faccioli; Fernanda Coeli-Lacchini; Juliana Gebenlian; Lays Sobral; Ayrton Moreira; Lucila Elias; Wilson Silva; Catr
http://abstracts.eurospe.org/hrp/0092/hrp0092RFC13.4
Published: 2019-08-22

88% match
16 hit(s)
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Loss-Of-Function NNT Mutations Impair Antioxidants Mechanisms and Decreases Cortisol Secretion in Patients with Famililar Glucocorticoid Deficieny | ESPE2019
Bodoni Aline Faccioli; Fernanda Coeli-Lacchini; Juliana Gebenlian; Lays Sobral; Ayrton Moreira; Lucila Elias; Wilson Silva; Catr
http://abstracts.eurospe.org/hrp/0092/hrp0092rfc13.4.html
Published: 2019-08-22

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