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UnknownRacial-Ethnic Differences in Treatment Initiation for New Diagnoses of Perinatal Depression.
Not available
S-EPMC10084773 | biostudies-literature
UnknownCongenital Hyperinsulinism and Evolution to Sulfonylurearesponsive Diabetes Later in Life due to a Novel Homozygous p.L171F ABCC8 Mutation
Not available
S-EPMC6398184 | biostudies-literature
UnknownClinical Characteristics, Molecular Features, and Long-Term Follow-Up of 15 Patients with Neonatal Diabetes: A Single-Centre Experience.
Not available
S-EPMC7611806 | biostudies-literature
UnknownNeonatal diabetes caused by a homozygous KCNJ11 mutation demonstrates that tiny changes in ATP sensitivity markedly affect diabetes risk.
Not available
S-EPMC4901145 | biostudies-literature
UnknownSavvyCNV: Genome-wide CNV calling from off-target reads.
Not available
S-EPMC8959187 | biostudies-literature
UnknownA type 1 diabetes genetic risk score can discriminate monogenic autoimmunity with diabetes from early-onset clustering of polygenic autoimmunity with diabetes.
Not available
S-EPMC6448971 | biostudies-literature
UnknownThe effect of early, comprehensive genomic testing on clinical care in neonatal diabetes: an international cohort study.
Not available
S-EPMC4772451 | biostudies-literature
UnknownType 1 Diabetes Genetic Risk Score: A Novel Tool to Discriminate Monogenic and Type 1 Diabetes.
Not available
S-EPMC4920219 | biostudies-literature
UnknownDe Novo Mutations in EIF2B1 Affecting eIF2 Signaling Cause Neonatal/Early-Onset Diabetes and Transient Hepatic Dysfunction.
Not available
S-EPMC7100014 | biostudies-literature
UnknownHomozygosity mapping provides supporting evidence of pathogenicity in recessive Mendelian disease.
Not available
S-EPMC6330071 | biostudies-literature
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