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

100% match
24 hit(s)
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27kb

Case Series; Experience of the Management of 2 Patients with Severe Anorexia Nervosa in Sligo University Hospital using the MARSIPAN protocol
Catherine McHugh; Ed O'Mahony; Mary Harron; Kilcullen Amanda
http://www.endocrine-abstracts.org/ea/0050/ea0050ep092.htm
Published: 2017-10-20

82% match
34 hit(s)
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Homozygous Loss-of-Function Mutation in the SLC26A7 Gene Coding a Novel Iodide Transporter Causes Goitrous Congenital Hypothyroidism | ESPE2019
Atsushi Suzuki; Jun Ishii; Aya Yoshida; Naoya Yamguchi; Tatsushi Tanaka; Kohei Aoyama; Michihiro Tateyama; I-Shan Chen; Yoshihir
http://abstracts.eurospe.org/hrp/0092/hrp0092FC5.6
Published: 2019-08-22

82% match
34 hit(s)
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Homozygous Loss-of-Function Mutation in the SLC26A7 Gene Coding a Novel Iodide Transporter Causes Goitrous Congenital Hypothyroidism | ESPE2019
Atsushi Suzuki; Jun Ishii; Aya Yoshida; Naoya Yamguchi; Tatsushi Tanaka; Kohei Aoyama; Michihiro Tateyama; I-Shan Chen; Yoshihir
http://abstracts.eurospe.org/hrp/0092/hrp0092fc5.6.html
Published: 2019-08-22

79% match
16 hit(s)
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A Novel SLC2A2 Mutation Implicated in Fanconi Bickel Syndrome and Dysglycemia | ESPE2019
Sanaa Sharari; Mustapha Aouida; Faiyaz Khan; Sara Al-Khawaga; Idris Mohammed; Basma Haris; Saras Saraswathi; Shihab Mundekkadan;
http://abstracts.eurospe.org/hrp/0092/hrp0092P1-189
Published: 2019-08-22

79% match
16 hit(s)
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A Novel SLC2A2 Mutation Implicated in Fanconi Bickel Syndrome and Dysglycemia | ESPE2019
Sanaa Sharari; Mustapha Aouida; Faiyaz Khan; Sara Al-Khawaga; Idris Mohammed; Basma Haris; Saras Saraswathi; Shihab Mundekkadan;
http://abstracts.eurospe.org/hrp/0092/hrp0092p1-189.html
Published: 2019-08-22

78% match
18 hit(s)
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Idiopathic Infantile Hypercalcemia: Mutations in SLC34A1 and CYP24A1 in Two Siblings and Fathers | ESPE2019
Ayla Güven; Martin Konrad; Karl Peter Schlingmann
http://abstracts.eurospe.org/hrp/0092/hrp0092P2-53
Published: 2019-08-22

78% match
18 hit(s)
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Idiopathic Infantile Hypercalcemia: Mutations in SLC34A1 and CYP24A1 in Two Siblings and Fathers | ESPE2019
Ayla Güven; Martin Konrad; Karl Peter Schlingmann
http://abstracts.eurospe.org/hrp/0092/hrp0092p2-53.html
Published: 2019-08-22

77% match
14 hit(s)
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Social Cognition Skills and Face Perception in Turner Syndrome (TS)
Vardit Gepstein; David Anaki; Tal Zadikov; Ze'ev Hochberg
http://abstracts.eurospe.org/hrp/0086/hrp0086fc6.6.htm
Published: 2016-08-19

76% match
16 hit(s)
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SOAR Study: New Approaches to Managing Social Skills Deficits in Turner Syndrome | ESPE2019
Jeanne Wolstencroft; Eleanor Kerry; Hayley Denyer; Alice Watkins; William Mandy; David Skuse
http://abstracts.eurospe.org/hrp/0092/hrp0092P1-375
Published: 2019-08-22

76% match
16 hit(s)
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SOAR Study: New Approaches to Managing Social Skills Deficits in Turner Syndrome | ESPE2019
Jeanne Wolstencroft; Eleanor Kerry; Hayley Denyer; Alice Watkins; William Mandy; David Skuse
http://abstracts.eurospe.org/hrp/0092/hrp0092p1-375.html
Published: 2019-08-22

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