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51. Exploring the potential of public proteomics data

52. A Hepatocyte Nuclear Factor-4α Gene (HNF4A) P2 Promoter Haplotype Linked With Late-Onset Diabetes

53. Permanent Neonatal Diabetes due to Mutations in KCNJ11 Encoding Kir6.2

54. The Chromosome 9p21 CVD- and T2D-Associated Regions in a Norwegian Population (The HUNT2 Survey)

55. Carboxyl-ester lipase maturity-onset diabetes of the young disease protein biomarkers in secretin-stimulated duodenal juice

56. Hyperphosphatemic familial tumoral calcinosis and hyperphosphatemic hyperostosis syndrome caused by a novel GALNT3 mutation; Long-term clinical outcome and phenotypic variability

57. Neurological Features and Enzyme Therapy in Patients With Endocrine and Exocrine Pancreas Dysfunction Due to CEL Mutations

58. Carboxyl-ester lipase maturity-onset diabetes of the young is associated with development of pancreatic cysts and upregulated MAPK signaling in secretin-stimulated duodenal fluid

59. Severe pancreatic dysfunction but compensated nutritional status in monogenic pancreatic disease caused by carboxyl-ester lipase mutations

60. Monogenic diabetes mellitus in Norway

61. Exocrine pancreatic function in hepatocyte nuclear factor 1β-maturity-onset diabetes of the young (HNF1B-MODY) is only moderately reduced: compensatory hypersecretion from a hypoplastic pancreas

62. Derivation of human induced pluripotent stem cells from patients with maturity onset diabetes of the young

63. Exome sequencing reveals FAM20c mutations associated with fibroblast growth factor 23-related hypophosphatemia, dental anomalies, and ectopic calcification

64. [Tailored medicine or narcissomics?]

65. Monogenic Phosphate Balance Disorders

66. The role of pancreatic imaging in monogenic diabetes mellitus

67. Diabetes and pancreatic exocrine dysfunction due to mutations in the carboxyl ester lipase gene-maturity onset diabetes of the young (CEL-MODY): a protein misfolding disease

68. HNF1B mutation in a Turkish child with renal and exocrine pancreas insufficiency, diabetes and liver disease

69. Evaluation of four novel genetic variants affecting hemoglobin A1c levels in a population-based type 2 diabetes cohort (the HUNT2 study)

70. [Progress in diabetes genetics]

71. Polygenic risk variants for type 2 diabetes susceptibility modify age at diagnosis in monogenic HNF1A diabetes

72. Pancreatic function in carboxyl-ester lipase knockout mice

73. Mutations in the VNTR of the carboxyl-ester lipase gene (CEL) are a rare cause of monogenic diabetes

74. A case of X-linked hypophosphatemic rickets: complications and the therapeutic use of cinacalcet

75. Reduced Pancreatic Volume in Hepatocyte Nuclear Factor 1A-Maturity-Onset Diabetes of the Young

76. Genetic analysis of recently identified type 2 diabetes loci in 1,638 unselected patients with type 2 diabetes and 1,858 control participants from a Norwegian population-based cohort (the HUNT study)

77. 50-year-old man with fatigue and monoclonal gammopaty

78. Pancreatic lipomatosis is a structural marker in nondiabetic children with mutations in carboxyl-ester lipase

79. A hepatocyte nuclear factor-4 alpha gene (HNF4A) P2 promoter haplotype linked with late-onset diabetes: studies of HNF4A variants in the Norwegian MODY registry

80. Mutations in the CEL VNTR cause a syndrome of diabetes and pancreatic exocrine dysfunction

81. Permanent neonatal diabetes due to mutations in KCNJ11 encoding Kir6.2: patient characteristics and initial response to sulfonylurea therapy

82. [Too narrow boot]

85. Secretin-stimulated duodenal markers associated with increased risk for pancreatic ductal adenocarcinoma

86. CEL-MODY causes both ductal and acinar pancreatic insufficiency

87. A case of X-linked hypophosphatemic rickets: complications and the therapeutic use of cinacalcet.

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