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Frontiers in Endocrinology
|
March 5, 2025
Large copy number variants are an important cause of congenital hyperinsulinism that should be screened for during routine testing
Sarah E Flanagan, Isabella-Anna Lazaridi, Jonna M E Männistö, et al.
Journal of Neuropathology and Experimental Neurology
|
April 16, 2026
Vascular burden attenuates the TDP-43-TMEM106B pathological relationship in neurodegenerative disease with and without Alzheimer disease neuropathological change
Matthew B Dopler, Cole Corbett, Angelique D Gonzalez, et al.
Autism Research : Official Journal of the International Society for Autism Research
|
January 12, 2019
Comparing the 1-year impact of preschool autism intervention programs in two Canadian provinces
Isabel M Smith, Helen E Flanagan, Wendy J Ungar, et al.
Journal of Clinical Immunology
|
January 4, 2023
FOXP3 TSDR Measurement Could Assist Variant Classification and Diagnosis of IPEX Syndrome
Rebecca C Wyatt, Sven Olek, Elisa De Franco, et al.
Diabetic Medicine : a Journal of the British Diabetic Association
|
June 16, 2010
Entities and frequency of neonatal diabetes: data from the diabetes documentation and quality management system (DPV)
J Grulich-Henn, V Wagner, A Thon, et al.
Diabetes
|
April 21, 2007
Mutations in ATP-sensitive K+ channel genes cause transient neonatal diabetes and permanent diabetes in childhood or adulthood
Sarah E Flanagan, Ann-Marie Patch, Deborah J G Mackay, et al.
British Journal of Cancer
|
June 16, 2005
Pharmacokinetically guided phase I trial of topotecan and etoposide phosphate in recurrent ovarian cancer
N C Levitt, D J Propper, S Madhusudan, et al.
Diabetic Medicine : a Journal of the British Diabetic Association
|
January 17, 2013
Biallelic PDX1 (insulin promoter factor 1) mutations causing neonatal diabetes without exocrine pancreatic insufficiency
E De Franco, C Shaw-Smith, S E Flanagan, et al.
Diabetologia
|
April 2, 2016
Successful transfer to sulfonylureas in KCNJ11 neonatal diabetes is determined by the mutation and duration of diabetes
Tarig Babiker, Natascia Vedovato, Kashyap Patel, et al.
Diabetologia
|
June 18, 2013
Improved genetic testing for monogenic diabetes using targeted next-generation sequencing
S Ellard, H Lango Allen, E De Franco, et al.
Page
of 59
Search research articles
Search
Showing results (401-410 of 582) with videos related to
Sort By:
Page
of 59
Frontiers in Endocrinology
|
March 5, 2025
Large copy number variants are an important cause of congenital hyperinsulinism that should be screened for during routine testing
Sarah E Flanagan, Isabella-Anna Lazaridi, Jonna M E Männistö, et al.
Journal of Neuropathology and Experimental Neurology
|
April 16, 2026
Vascular burden attenuates the TDP-43-TMEM106B pathological relationship in neurodegenerative disease with and without Alzheimer disease neuropathological change
Matthew B Dopler, Cole Corbett, Angelique D Gonzalez, et al.
Autism Research : Official Journal of the International Society for Autism Research
|
January 12, 2019
Comparing the 1-year impact of preschool autism intervention programs in two Canadian provinces
Isabel M Smith, Helen E Flanagan, Wendy J Ungar, et al.
Journal of Clinical Immunology
|
January 4, 2023
FOXP3 TSDR Measurement Could Assist Variant Classification and Diagnosis of IPEX Syndrome
Rebecca C Wyatt, Sven Olek, Elisa De Franco, et al.
Diabetic Medicine : a Journal of the British Diabetic Association
|
June 16, 2010
Entities and frequency of neonatal diabetes: data from the diabetes documentation and quality management system (DPV)
J Grulich-Henn, V Wagner, A Thon, et al.
Diabetes
|
April 21, 2007
Mutations in ATP-sensitive K+ channel genes cause transient neonatal diabetes and permanent diabetes in childhood or adulthood
Sarah E Flanagan, Ann-Marie Patch, Deborah J G Mackay, et al.
British Journal of Cancer
|
June 16, 2005
Pharmacokinetically guided phase I trial of topotecan and etoposide phosphate in recurrent ovarian cancer
N C Levitt, D J Propper, S Madhusudan, et al.
Diabetic Medicine : a Journal of the British Diabetic Association
|
January 17, 2013
Biallelic PDX1 (insulin promoter factor 1) mutations causing neonatal diabetes without exocrine pancreatic insufficiency
E De Franco, C Shaw-Smith, S E Flanagan, et al.
Diabetologia
|
April 2, 2016
Successful transfer to sulfonylureas in KCNJ11 neonatal diabetes is determined by the mutation and duration of diabetes
Tarig Babiker, Natascia Vedovato, Kashyap Patel, et al.
Diabetologia
|
June 18, 2013
Improved genetic testing for monogenic diabetes using targeted next-generation sequencing
S Ellard, H Lango Allen, E De Franco, et al.
Page
of 59