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American Journal of Human Genetics
|
January 13, 2000
Elevated levels of FMR1 mRNA in carrier males: a new mechanism of involvement in the fragile-X syndrome
F Tassone, R J Hagerman, A K Taylor, et al.
American Journal of Medical Genetics
|
April 20, 1999
Compound heterozygous female with fragile X syndrome
M G Linden, F Tassone, L W Gane, et al.
Journal of Medical Genetics
|
December 7, 2007
A low symptomatic form of neurodegeneration in younger carriers of the FMR1 premutation, manifesting typical radiological changes
D Z Loesch, M Cook, L Litewka, et al.
Journal of Endocrinological Investigation
|
January 2, 2003
The nutritional status has no major role in the age-related reduction of IGF-I secretion
C Baffoni, A Benso, F Broglio, et al.
Journal of Endocrinological Investigation
|
March 10, 2005
A rare case of adulthood-onset growth hormone deficiency presenting as sporadic, symptomatic hypoglycemia
A Pia, A Piovesan, F Tassone, et al.
Paediatric Anaesthesia
|
August 28, 2009
Acupuncture management of pain and emergence agitation in children after bilateral myringotomy and tympanostomy tube insertion
Yuan-Chi Lin, Rosalie F Tassone, Stefan Jahng, et al.
Clinical Endocrinology
|
December 18, 2003
Obese patients with obstructive sleep apnoea syndrome show a peculiar alteration of the corticotroph but not of the thyrotroph and lactotroph function
F Lanfranco, L Gianotti, S Pivetti, et al.
The Clinical Neuropsychologist
|
June 30, 2016
Broad autism spectrum and obsessive-compulsive symptoms in adults with the fragile X premutation
A Schneider, C Johnston, F Tassone, et al.
Journal of Endocrinological Investigation
|
December 23, 2011
Prevalence and characteristics of metabolic syndrome in primary hyperparathyroidism
F Tassone, L Gianotti, C Baffoni, et al.
Endocrine
|
September 26, 2013
Insulin sensitivity in normocalcaemic primary hyperparathyroidism
F Tassone, M Maccario, L Gianotti, et al.
Page
of 13
Search research articles
Search
Showing results (71-80 of 129) with videos related to
Sort By:
Page
of 13
American Journal of Human Genetics
|
January 13, 2000
Elevated levels of FMR1 mRNA in carrier males: a new mechanism of involvement in the fragile-X syndrome
F Tassone, R J Hagerman, A K Taylor, et al.
American Journal of Medical Genetics
|
April 20, 1999
Compound heterozygous female with fragile X syndrome
M G Linden, F Tassone, L W Gane, et al.
Journal of Medical Genetics
|
December 7, 2007
A low symptomatic form of neurodegeneration in younger carriers of the FMR1 premutation, manifesting typical radiological changes
D Z Loesch, M Cook, L Litewka, et al.
Journal of Endocrinological Investigation
|
January 2, 2003
The nutritional status has no major role in the age-related reduction of IGF-I secretion
C Baffoni, A Benso, F Broglio, et al.
Journal of Endocrinological Investigation
|
March 10, 2005
A rare case of adulthood-onset growth hormone deficiency presenting as sporadic, symptomatic hypoglycemia
A Pia, A Piovesan, F Tassone, et al.
Paediatric Anaesthesia
|
August 28, 2009
Acupuncture management of pain and emergence agitation in children after bilateral myringotomy and tympanostomy tube insertion
Yuan-Chi Lin, Rosalie F Tassone, Stefan Jahng, et al.
Clinical Endocrinology
|
December 18, 2003
Obese patients with obstructive sleep apnoea syndrome show a peculiar alteration of the corticotroph but not of the thyrotroph and lactotroph function
F Lanfranco, L Gianotti, S Pivetti, et al.
The Clinical Neuropsychologist
|
June 30, 2016
Broad autism spectrum and obsessive-compulsive symptoms in adults with the fragile X premutation
A Schneider, C Johnston, F Tassone, et al.
Journal of Endocrinological Investigation
|
December 23, 2011
Prevalence and characteristics of metabolic syndrome in primary hyperparathyroidism
F Tassone, L Gianotti, C Baffoni, et al.
Endocrine
|
September 26, 2013
Insulin sensitivity in normocalcaemic primary hyperparathyroidism
F Tassone, M Maccario, L Gianotti, et al.
Page
of 13