|
1
|
Insulin gene mutations as a cause of permanent neonatal diabetes.
|
Proc Natl Acad Sci U S A
|
2007
|
3.77
|
|
2
|
Sulfonylurea treatment before genetic testing in neonatal diabetes: pros and cons.
|
J Clin Endocrinol Metab
|
2014
|
3.07
|
|
3
|
Educating future leaders of medical research: analysis of student opinions and goals from the MD-PhD SAGE (Students' Attitudes, Goals, and Education) survey.
|
Acad Med
|
2007
|
2.35
|
|
4
|
Educational views and attitudes, and career goals of MD-PhD students at the University of Pennsylvania School of Medicine.
|
Acad Med
|
2005
|
2.13
|
|
5
|
Diagnosis and treatment of neonatal diabetes: a United States experience.
|
Pediatr Diabetes
|
2008
|
1.55
|
|
6
|
MD-PhD students in a major training program show strong interest in becoming surgeon-scientists.
|
Clin Orthop Relat Res
|
2004
|
1.28
|
|
7
|
Neonatal diabetes, gallbladder agenesis, duodenal atresia, and intestinal malrotation caused by a novel homozygous mutation in RFX6.
|
Pediatr Diabetes
|
2013
|
1.22
|
|
8
|
Age at the time of sulfonylurea initiation influences treatment outcomes in KCNJ11-related neonatal diabetes.
|
Diabetologia
|
2015
|
0.99
|
|
9
|
Tooth discoloration in patients with neonatal diabetes after transfer onto glibenclamide: a previously unreported side effect.
|
Diabetes Care
|
2009
|
0.97
|
|
10
|
Cost-effectiveness of MODY genetic testing: translating genomic advances into practical health applications.
|
Diabetes Care
|
2013
|
0.94
|
|
11
|
Visuomotor performance in KCNJ11-related neonatal diabetes is impaired in children with DEND-associated mutations and may be improved by early treatment with sulfonylureas.
|
Diabetes Care
|
2012
|
0.88
|
|
12
|
HLA-DQ haplotypes differ by ethnicity in patients with childhood-onset diabetes.
|
Pediatr Diabetes
|
2011
|
0.86
|
|
13
|
Successful transition from insulin to sulfonylurea therapy in a patient with monogenic neonatal diabetes owing to a KCNJ11 F333L [corrected] mutation.
|
Diabetes Care
|
2013
|
0.80
|
|
14
|
Microcephaly, epilepsy, and neonatal diabetes due to compound heterozygous mutations in IER3IP1: insights into the natural history of a rare disorder.
|
Pediatr Diabetes
|
2013
|
0.76
|
|
15
|
Extremely Early Onset IPEX Syndrome Caused by a Novel Small Exonic Deletion in FOXP3.
|
J Pediatr Gastroenterol Nutr
|
2016
|
0.75
|
|
16
|
Genomic sequencing in newborn screening programs.
|
JAMA
|
2012
|
0.75
|
|
17
|
Hyperinsulinism in a neonate.
|
Pediatr Ann
|
2014
|
0.75
|
|
18
|
The Effect of the Testis on the Ovary: Structure-Function Relationships in a Neonate with a Unilateral Ovotestis (Ovotesticular Disorder of Sex Development)
.
|
Horm Res Paediatr
|
2017
|
0.75
|