Lerone M - Search Results

1

Fontaine-Farriaux craniosynostosis: second report in the literature.

Priolo M, De Toni T, Baffico M, Cama A, Seri M, Cusano R, Costabello L, Fondelli P, Capra V, Silengo M, Ravazzolo R, Lerone M. Priolo M, et al. Among authors: lerone m. Am J Med Genet. 2001 May 1;100(3):214-8. Am J Med Genet. 2001. PMID: 11343306

2

Autosomal recessive microcephaly with early onset seizures and spasticity.

Silengo M, Lerone M, Martinelli M, Martucciello G, Caffarena PE, Jasonni V, Romeo G. Silengo M, et al. Among authors: lerone m. Clin Genet. 1992 Sep;42(3):152-5. doi: 10.1111/j.1399-0004.1992.tb03228.x. Clin Genet. 1992. PMID: 1395086

3

Congenital diaphragmatic hernia associated with ipsilateral upper limb reduction defects: report of a case with thumb hypoplasia.

Lerone M, Soliani M, Corea D, Romeo G, Martucciello G, Silengo MC. Lerone M, et al. Am J Med Genet. 1992 Dec 1;44(6):827-9. doi: 10.1002/ajmg.1320440623. Am J Med Genet. 1992. PMID: 1481856

4

Oculocerebral syndrome with hypopigmentation (Cross syndrome): report of a new case.

Lerone M, Pessagno A, Taccone A, Poggi G, Romeo G, Silengo MC. Lerone M, et al. Clin Genet. 1992 Feb;41(2):87-9. doi: 10.1111/j.1399-0004.1992.tb03639.x. Clin Genet. 1992. PMID: 1544218

5

Leiomyomatosis of oesophagus, congenital cataracts and hematuria. Report of a case with rectal involvement.

Lerone M, Dodero P, Romeo G, Martucciello G, Caffarena PE, Brisigotti M, Toma P, Taccone A, Silengo M. Lerone M, et al. Pediatr Radiol. 1991;21(8):578-9. doi: 10.1007/BF02012602. Pediatr Radiol. 1991. PMID: 1815180

6

Multiple sutural synostosis and congenital cataracts.

Lerone M, Romeo G, Conrad E, Silvano S, Cama A, Silengo CM. Lerone M, et al. Hum Genet. 1991 Oct;87(6):758. doi: 10.1007/BF00201745. Hum Genet. 1991. PMID: 1937484 No abstract available.

7

A new syndrome with cerebro-oculo-skeletal-renal involvement.

Silengo MC, Lerone M, Pelizza A, Gatti R, Barabino A, Romeo G. Silengo MC, et al. Among authors: lerone m. Pediatr Radiol. 1990;20(8):612-4. doi: 10.1007/BF02129073. Pediatr Radiol. 1990. PMID: 2251013

8

Heterogeneity and low detection rate of RET mutations in Hirschsprung disease.

Yin L, Barone V, Seri M, Bolino A, Bocciardi R, Ceccherini I, Pasini B, Tocco T, Lerone M, Cywes S, et al. Yin L, et al. Among authors: lerone m. Eur J Hum Genet. 1994;2(4):272-80. doi: 10.1159/000472371. Eur J Hum Genet. 1994. PMID: 7704557

9

Point mutations affecting the tyrosine kinase domain of the RET proto-oncogene in Hirschsprung's disease.

Romeo G, Ronchetto P, Luo Y, Barone V, Seri M, Ceccherini I, Pasini B, Bocciardi R, Lerone M, Kääriäinen H, et al. Romeo G, et al. Among authors: lerone m. Nature. 1994 Jan 27;367(6461):377-8. doi: 10.1038/367377a0. Nature. 1994. PMID: 8114938

10

Uncombable hair, retinal pigmentary dystrophy, dental anomalies, and brachydactyly: report of a new patient with additional findings.

Silengo M, Lerone M, Romeo G, Calcagno E, Martucciello G, Jasonni V. Silengo M, et al. Among authors: lerone m. Am J Med Genet. 1993 Nov 1;47(6):931-3. doi: 10.1002/ajmg.1320470624. Am J Med Genet. 1993. PMID: 8279493

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