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| 1 | An official ATS clinical policy statement: congenital central hypoventilation syndrome: genetic basis, diagnosis, and management 显示文摘 | Weese-Mayer DE Berry-Kravis EM Ceccherini I | 2010 | Am J Respir Crit Care Med2010，181，6： | 1 |
| 2 | Pathogenesis of Hirsehsprung's disease显示文摘 | Martucciello G Ceccherini I Lerone M Jasonni V | 2000 | J Pediatr Surg2000，35，： | 1 |
| 3 | An official ATS clinical policy statement:congenital central hypoventilation syndrome:genetic basis,diagnosis,and management显示文摘 | Weese-Mayer DE Berry-Kravis EM Ceccherini I | | American Journal of Respiratory and Critical Care Medicine0，，： | 1 |
| 4 | Incidence of RET mutations in patients with Hirschsprung's disease显示文摘 | Sancandi M Ceccherini I Costa M | 2000 | J Pediatr Surg2000，35，1： | 1 |
| 5 | Congenital central hypoventilation syndrome (CCHS) and sudden infant death syndrome (SIDS) : kindred disorders of autonomic regulation 显示文摘 | Weese DE Berry EM Ceccherini I | 2008 | Respir Physiol Neurobiol2008，164，1： | 1 |
| 6 | A mutation in theRET proto-oncogene associated with multiple endocrine neoplasiatype 26 and sporadic medullary thyroid carcinoma 显示文摘 | Hofstra RM Landsvater RM Ceccherini I | 1994 | Nature1994，367，6461： | 1 |
| 7 | Congenital central hypoventilation syndrome(CCHS) and sudden infant death syndrome (SIDS):kindred disorders of autonomic regulation显示文摘 | Weese DE Berry EM Ceccherini I | 2008 | Respir Physiol Neurobiol2008，164，1： | 1 |
| 8 | An official ATS clinical policy statement:congenital central hypoventilation syndrome:genetic basis, diagnosis, and management显示文摘 | Weese Mayer DE Berry Kravis EM Ceccherini I | 2010 | Am J Respir Crit Care Med2010，181，： | 1 |
| 9 | Hirschsprung disease and congenital anomalies of the kidney and urinary tract (CAKUT):a novel syndromic association显示文摘 | Pini Prato A Musso M Ceccherini I | 2009 | Medicine (Baltimore)2009，88，2： | 1 |
| 10 | A mutation in the RET protooncogene associated with MEN2B and sporadic me- dullary carcinoma显示文摘 | Hofstra RM Landsvater RM Ceccherini I | 1994 | Nature1994，367，6461： | 1 |
| 11 | Pathogenesis of Hirschsprong's disease 显示文摘 | Martucciello G Ceccherini I Lerone M | 2000 | J Pediatr Surg2000，35，7： | 1 |
| 12 | Molecular mechanisms of RET-induced Hirschsprung pathogenesis显示文摘 | Lantieri F Griseri P Ceccherini I | 2006 | Ann Med2006，38，1： | 1 |
| 13 | A mutation in the RET proto-oncogene associated with muhip|e endocrine neoplasia type2B and sporadic medullary thyroid carcinoma显示文摘 | Hofstra RM Landsvater RM Ceccherini I | 1994 | Nature1994，367，6461： | 1 |
| 14 | RET mutations in human disease显示文摘 | Pasini B Ceccherini I Romeo G | 1996 | Trends Genet1996，12，： | 1 |
| 15 | Incidence of RET mutations in patients with Hirschsprung's disease 显示文摘 | Sancandi M Ceccherini I Costa M | 2000 | J Pediatr Surg2000，35，1： | 1 |
| 16 | An official ATS clinical policy statement: congenital central hypoventilatlon syndrome: genetic basis, diagnosis, and management 显示文摘 | Weese-Mayer DE Berry-Kravis EM Ceccherini I | 2010 | Am J Respir Crit Care Med2010，181，6： | 1 |
| 17 | An official ATS clinical policy statement : Congenital centrai hypoventilation syndrome: genetic basis, diagnosis, and management 显示文摘 | Weese-Mayer DE Berry-Kravis EM Ceccherini I | 2010 | Am J Respir Crit Care Med2010，181，6： | 1 |
| 18 | A mutation in the RET protooncogene associated with MEN2B and sporadic medullary carcinoma显示文摘 | Hofstra RM Landsvater RM Ceccherini I | 1994 | Nature1994，367，6461： | 1 |
| 19 | A mutation in the RET proto-oncogene associated with multiple endocrine neoplasia type 2B and sporadic medullary thyroid carcinoma显示文摘 | Hofstra RM Landsvater RM Ceccherini I | 1994 | Nature1994，367，6461： | 1 |
| 20 | A mutation in the RET proto-oncogene associated with multiple endocrine neoplasia type 2B and sproadic medullary throid carcinoma显示文摘 | Hofstra RM Landsvater RM Ceccherini I | | 0，，： | 1 |
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