Boldrini R - Search Results

1

Fatal infantile leukodystrophy: a severe variant of CACH/VWM syndrome, allelic to chromosome 3q27.

Francalanci P, Eymard-Pierre E, Dionisi-Vici C, Boldrini R, Piemonte F, Virgili R, Fariello G, Bosman C, Santorelli FM, Boespflug-Tanguy O, Bertini E. Francalanci P, et al. Among authors: boldrini r. Neurology. 2001 Jul 24;57(2):265-70. doi: 10.1212/wnl.57.2.265. Neurology. 2001. PMID: 11468311

2

Clinical and molecular findings in hyperornithinemia-hyperammonemia-homocitrullinuria syndrome.

Salvi S, Santorelli FM, Bertini E, Boldrini R, Meli C, Donati A, Burlina AB, Rizzo C, Di Capua M, Fariello G, Dionisi-Vici C. Salvi S, et al. Among authors: boldrini r. Neurology. 2001 Sep 11;57(5):911-4. doi: 10.1212/wnl.57.5.911. Neurology. 2001. PMID: 11552031

3

Novel large-range mitochondrial DNA deletions and fatal multisystemic disorder with prominent hepatopathy.

Bianchi M, Rizza T, Verrigni D, Martinelli D, Tozzi G, Torraco A, Piemonte F, Dionisi-Vici C, Nobili V, Francalanci P, Boldrini R, Callea F, Santorelli FM, Bertini E, Carrozzo R. Bianchi M, et al. Among authors: boldrini r. Biochem Biophys Res Commun. 2011 Nov 18;415(2):300-4. doi: 10.1016/j.bbrc.2011.10.049. Epub 2011 Oct 18. Biochem Biophys Res Commun. 2011. PMID: 22027147 Free PMC article.

4

The use of muscle biopsy in the diagnosis of undefined ataxia with cerebellar atrophy in children.

Terracciano A, Renaldo F, Zanni G, D'Amico A, Pastore A, Barresi S, Valente EM, Piemonte F, Tozzi G, Carrozzo R, Valeriani M, Boldrini R, Mercuri E, Santorelli FM, Bertini E. Terracciano A, et al. Among authors: boldrini r. Eur J Paediatr Neurol. 2012 May;16(3):248-56. doi: 10.1016/j.ejpn.2011.07.016. Epub 2011 Aug 27. Eur J Paediatr Neurol. 2012. PMID: 21873089 Free PMC article.

5

Unusual aspects of desmoplastic small round cell tumor.

Bosman C, Boldrini R. Bosman C, et al. Among authors: boldrini r. Ultrastruct Pathol. 2004 Mar-Apr;28(2):83-96. doi: 10.1080/01913120490430634. Ultrastruct Pathol. 2004. PMID: 15205108

6

Involvement of respiratory muscles in cytoplasmic body myopathy--a pathology study.

Bertini E, Ricci E, Boldrini R, Servidei S, Fusilli S, Dionisi-Vici C, Bosman C, Bonilla E. Bertini E, et al. Among authors: boldrini r. Brain Dev. 1990;12(6):798-806. doi: 10.1016/s0387-7604(12)80010-6. Brain Dev. 1990. PMID: 2092592

7

Dilated cardiomyopathy in infancy. Ultrastructural image analysis for diagnostic purpose.

Bosman C, Boldrini R, Fusilli S. Bosman C, et al. Among authors: boldrini r. Pathol Res Pract. 1989 Nov;185(5):807-17. doi: 10.1016/S0344-0338(89)80245-6. Pathol Res Pract. 1989. PMID: 2626394

8

Tachycardias in children originating in the right ventricular outflow tract: lack of clinical features predicting the presence and severity of the histopathological substrate.

Drago F, Mazza A, Gagliardi MG, Bevilacqua M, Di Renzi P, Calzolari A, Francalanci P, Boldrini R, Bosman C, Di Liso G, Ragonese P. Drago F, et al. Among authors: boldrini r. Cardiol Young. 1999 May;9(3):273-9. doi: 10.1017/s1047951100004935. Cardiol Young. 1999. PMID: 10386696

9

[Wolman's disease: a case with malabsorption and 2 cases with virus- negative fatty liver cirrhosis].

Boldrini R, Castro M, Marcellini M, Piemonte F, Bosman C. Boldrini R, et al. Pathologica. 2000 Apr;92(2):130-1. Pathologica. 2000. PMID: 10838887 Italian. No abstract available.

10

Pierre Robin syndrome and Wilms tumor: an unusual association.

Camassei FD, Jenkner A, Bertini E, Bosman C, Donfrancesco A, Boldrini R. Camassei FD, et al. Among authors: boldrini r. Med Pediatr Oncol. 2000 Jul;35(1):83-4. doi: 10.1002/1096-911x(200007)35:1<83::aid-mpo16>3.0.co;2-t. Med Pediatr Oncol. 2000. PMID: 10881015 No abstract available.

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