1
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Incremental value of continuous glucose monitoring when starting pump therapy in patients with poorly controlled type 1 diabetes: the RealTrend study.
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Diabetes Care
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2009
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2.84
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2
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The type and the position of HNF1A mutation modulate age at diagnosis of diabetes in patients with maturity-onset diabetes of the young (MODY)-3.
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Diabetes
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2007
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1.65
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3
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Perilipin deficiency and autosomal dominant partial lipodystrophy.
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N Engl J Med
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2011
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1.61
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4
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Novel mutations of the PCSK9 gene cause variable phenotype of autosomal dominant hypercholesterolemia.
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Hum Mutat
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2005
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1.54
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5
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Anti-thyroperoxidase antibodies from patients with Hashimoto's encephalopathy bind to cerebellar astrocytes.
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J Neuroimmunol
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2007
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1.47
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6
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PIK3R1 mutations cause syndromic insulin resistance with lipoatrophy.
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Am J Hum Genet
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2013
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1.33
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7
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New metabolic phenotypes in laminopathies: LMNA mutations in patients with severe metabolic syndrome.
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J Clin Endocrinol Metab
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2007
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1.27
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8
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Macroscopic lymph-node involvement and neck dissection predict lymph-node recurrence in papillary thyroid carcinoma.
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Eur J Endocrinol
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2008
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1.25
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9
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OpT2mise: a randomized controlled trial to compare insulin pump therapy with multiple daily injections in the treatment of type 2 diabetes-research design and methods.
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Diabetes Technol Ther
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2014
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1.24
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10
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Intronic mutations outside of Alu-repeat-rich domains of the LDL receptor gene are a cause of familial hypercholesterolemia.
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Hum Genet
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2002
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1.14
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11
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Clinical characteristics and diagnostic criteria of maturity-onset diabetes of the young (MODY) due to molecular anomalies of the HNF1A gene.
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J Clin Endocrinol Metab
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2011
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1.10
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12
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Abnormal sensitivity of cortisol-producing adrenocortical adenomas to serotonin: in vivo and in vitro studies.
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J Clin Endocrinol Metab
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2005
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1.05
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13
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F18-choline, a novel PET tracer for parathyroid adenoma?
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J Clin Endocrinol Metab
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2013
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1.05
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14
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Ectopic ACTH syndrome in children and adolescents.
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J Clin Endocrinol Metab
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2011
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1.01
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15
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Dual-phase 99mTc sestamibi scintigraphy with neck and thorax SPECT/CT in primary hyperparathyroidism: a single-institution experience.
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Clin Nucl Med
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2012
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0.99
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16
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McCune-Albright syndrome and acromegaly: effects of hypothalamopituitary radiotherapy and/or pegvisomant in somatostatin analog-resistant patients.
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J Clin Endocrinol Metab
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2006
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0.94
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17
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Clinical and metabolic features of adult-onset diabetes caused by ABCC8 mutations.
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Diabetes Care
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2011
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0.84
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18
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Clinical and biochemical characteristics of normotensive patients with primary aldosteronism: a comparison with hypertensive cases.
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Clin Endocrinol (Oxf)
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2008
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0.84
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19
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Evaluation of endocrine testing of Leydig cell function using extractive and recombinant human chorionic gonadotropin and different doses of recombinant human LH in normal men.
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Eur J Endocrinol
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2008
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0.82
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20
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"Rescue" bilateral adrenalectomy in paraneoplastic Cushing's syndrome with invasive Aspergillus fumigatus infection.
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Am J Med Sci
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2007
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0.81
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21
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A homozygous mutation of prelamin-A preventing its farnesylation and maturation leads to a severe lipodystrophic phenotype: new insights into the pathogenicity of nonfarnesylated prelamin-A.
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J Clin Endocrinol Metab
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2011
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0.81
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22
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Major hyperestrogenism in a feminizing adrenocortical adenoma despite a moderate overexpression of the aromatase enzyme.
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Eur J Endocrinol
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2003
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0.81
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23
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Transient pituitary enlargement with central hypogonadism secondary to bilateral cavernous sinus thrombosis: pituitary oedema?
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Eur J Endocrinol
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2009
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0.81
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24
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Neuromuscular electrostimulation and insulin sensitivity in patients with type 2 diabetes: the ELECTRODIAB pilot study.
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Acta Diabetol
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2014
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0.81
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25
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BMP system expression in GCs from polycystic ovary syndrome women and the in vitro effects of BMP4, BMP6, and BMP7 on GC steroidogenesis.
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Eur J Endocrinol
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2013
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0.80
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26
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Cushing's syndrome associated with a nested stromal epithelial tumor of the liver: hormonal, immunohistochemical, and molecular studies.
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Eur J Endocrinol
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2009
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0.80
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27
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Case report: cushing disease caused by an ectopic intracavernous pituitary microadenoma: case report and review of the literature.
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J Comput Assist Tomogr
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2003
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0.78
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28
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Aromatase expression in the normal human adult adrenal and in adrenocortical tumors: biochemical, immunohistochemical, and molecular studies.
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Eur J Endocrinol
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2008
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0.77
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29
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The clinical spectrum of RET proto-oncogene mutations in codon 790.
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Eur J Endocrinol
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2013
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0.75
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30
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Hypoglycaemia in adults: when should it be raised? How can hypoglycaemia be confirmed in non-diabetic adults?
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Ann Endocrinol (Paris)
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2013
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0.75
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31
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Personalization of a compartmental physiological model for an artificial pancreas through integration of patient's state estimation.
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Conf Proc IEEE Eng Med Biol Soc
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2017
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0.75
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32
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Aberrant adrenal sensitivity to vasopressin in adrenal tumours associated with subclinical or overt autonomous hypercortisolism: is this explained by an overexpression of vasopressin receptors?
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Clin Endocrinol (Oxf)
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2007
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0.75
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33
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Paraneoplastic ACTH secretion: bronchial carcinoid overlooked by planar indium-111 pentetreotide scintigraphy and accurately localized by SPECT/CT acquisition.
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Clin Nucl Med
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2007
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0.75
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34
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Dextrose infusion and glucose disorders in people without diabetes hospitalized in general wards.
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Diabetes Res Clin Pract
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2013
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0.75
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