14 results on '"De Sanctis, L."'
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2. Autoimmune polyendocrine syndrome type 1: an Italian survey on 158 patients
3. X-linked hypophosphatemic rickets: an Italian experts’ opinion survey
4. Screening for mutations in the ISL1 gene in patients with thyroid dysgenesis
5. Mutations in TAZ/WWTR1, a co-activator of NKX2.1 and PAX8 are not a frequent cause of thyroid dysgenesis
6. GH secretion in a cohort of children with pseudohypoparathyroidism type Ia
7. On the “Matrix Approach” to Interacting Particle Systems
8. Genotype–phenotype correlation in dihydropteridine reductase deficiency
9. Application of Prastat ELISA in the determination of anti-HLA specificity for immunized patients awaiting kidney transplant: five years' experience
10. Clinical heterogeneity of familial pseudohypoparathyroidism
11. Prospective study of the detection and treatment of small tumors of the head of the pancreas
12. Phenotyping of phenylketonuric patients by oral phenylalanine loading
13. Monitoring treatment in tetrahydrobiopterin deficiency by serum prolactin
14. Phenotype characterization and prevalence of rBAT M467T mutation in Italian cystinuric patients
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