Multiple endocrine neoplasia type 1: extensive analysis of a large database of Florentine patients

Multiple endocrine neoplasia type 1: extensive analysis of a large database of Florentine patients is …
instance of (P31):
scholarly articleQ13442814

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P6179Dimensions Publication ID1109899763
P356DOI10.1186/S13023-018-0938-8
P932PMC publication ID6237029
P698PubMed publication ID30428914

P50authorMaria Luisa BrandiQ29839820
P2093author name stringFrancesca Marini
Francesca Giusti
P2860cites workGender-related differences in MEN1 lesion occurrence and diagnosis: a cohort study of 734 cases from the Groupe d'etude des Tumeurs Endocrines.Q51466728
Long-Term Natural Course of Pituitary Tumors in Patients With MEN1: Results From the DutchMEN1 Study Group (DMSG).Q53446846
Multiple endocrine neoplasia type 1: analysis of germline MEN1 mutations in the Italian multicenter MEN1 patient databaseQ56927393
Higher risk of death among MEN1 patients with mutations in the JunD interacting domain: a Groupe d’étude des Tumeurs Endocrines (GTE) cohort studyQ61647410
Pituitary tumors and hyperplasia in multiple endocrine neoplasia type 1 syndrome (MEN1): a case-control study in a series of 77 patients versus 2509 non-MEN1 patientsQ80775138
Cinacalcet therapy in patients affected by primary hyperparathyroidism associated to Multiple Endocrine Neoplasia Syndrome type 1 (MEN1)Q85675298
MEN1 disease occurring before 21 years old: a 160-patient cohort study from the Groupe d'étude des Tumeurs EndocrinesQ86546147
Multiple endocrine neoplasia type 1 (MEN1): analysis of 1336 mutations reported in the first decade following identification of the geneQ28249576
Epidemiology data on 108 MEN 1 patients from the GTE with isolated nonfunctioning tumors of the pancreasQ31030383
Multiple endocrine neoplasia syndrome type 1: institution, management, and data analysis of a nationwide multicenter patient databaseQ31157584
Clinical practice guidelines for multiple endocrine neoplasia type 1 (MEN1).Q34283436
Variable clinical expression in patients with a germline MEN1 disease gene mutation: clues to a genotype-phenotype correlation.Q35895504
MEN1 in children and adolescents: Data from patients of a regional referral center for hereditary endocrine tumorsQ36377417
Primary hyperparathyroidism in MEN1 patients: a cohort study with longterm follow-up on preferred surgical procedure and the relation with genotypeQ37999297
Multiple endocrine neoplasia type 1 (MEN1): An update of 208 new germline variants reported in the last nine years.Q38696748
PROGNOSTIC FACTORS FOR SURVIVAL OF MEN1 PATIENTS WITH DUODENOPANCREATIC TUMORS METASTATIC TO THE LIVER: RESULTS FROM THE DMSG.Q40324106
Unraveling the intrafamilial correlations and heritability of tumor types in MEN1: a Groupe d'étude des Tumeurs Endocrines studyQ40516484
Multiple endocrine neoplasia type 1 in Japan: establishment and analysis of a multicentre databaseQ43840894
Risk factors and causes of death in MEN1 disease. A GTE (Groupe d'Etude des Tumeurs Endocrines) cohort study among 758 patientsQ44301609
The genetic ascertainment of multiple endocrine neoplasia type 1 syndrome by ancient DNA analysis.Q47632021
P275copyright licenseCreative Commons Attribution 4.0 InternationalQ20007257
P6216copyright statuscopyrightedQ50423863
P433issue1
P407language of work or nameEnglishQ1860
P921main subjectmultiple endocrine neoplasiaQ1553018
multiple endocrine neoplasia type 1Q3347154
P304page(s)205
P577publication date2018-11-14
P1433published inOrphanet Journal of Rare DiseasesQ15756117
P1476titleMultiple endocrine neoplasia type 1: extensive analysis of a large database of Florentine patients
P478volume13

Reverse relations

Q90310150MEN1-associated primary hyperparathyroidism in the Spanish Registry: clinical characterictics and surgical outcomescites workP2860