Parenti G - Search Results

1

Increased prevalence of thyroid autoimmunity and hypothyroidism in patients with glycogen storage disease type I.

Melis D, Pivonello R, Parenti G, Della Casa R, Salerno M, Lombardi G, Sebastio G, Colao A, Andria G. Melis D, et al. Among authors: parenti g. J Pediatr. 2007 Mar;150(3):300-5, 305.e1. doi: 10.1016/j.jpeds.2006.11.056. J Pediatr. 2007. PMID: 17307551

2

Dietary treatment of liver glycogenosis.

Andria G, Parenti G, Strisciuglio P, Tinello C. Andria G, et al. Among authors: parenti g. Beitr Infusionsther. 1991;27:161-9. Beitr Infusionsther. 1991. PMID: 1713097 Review. No abstract available.

3

Evidence of polyglandular involvement in Niemann-Pick disease type B.

Strisciuglio P, Di Maio S, Parenti G, Franzese A, Lubrano P, Mariano A, Andria G. Strisciuglio P, et al. Among authors: parenti g. Eur J Pediatr. 1987 Jul;146(4):431-3. doi: 10.1007/BF00444957. Eur J Pediatr. 1987. PMID: 2820735

4

Studies on cross-reacting material to steroid sulphatase in fibroblasts from patients affected by different types of steroid sulphatase deficiency.

Parenti G, Ballabio A, Hoogeveen AT, Van der Loos CM, Jobsis AC, Andria G. Parenti G, et al. J Inherit Metab Dis. 1987;10(3):224-8. doi: 10.1007/BF01800065. J Inherit Metab Dis. 1987. PMID: 3123779

5

X/Y translocation in a family with X-linked ichthyosis, chondrodysplasia punctata, and mental retardation: DNA analysis reveals deletion of the steroid sulphatase gene and translocation of its Y pseudogene.

Ballabio A, Parenti G, Carrozzo R, Coppa G, Felici L, Migliori V, Silengo M, Franceschini P, Andria G. Ballabio A, et al. Among authors: parenti g. Clin Genet. 1988 Jul;34(1):31-7. doi: 10.1111/j.1399-0004.1988.tb02612.x. Clin Genet. 1988. PMID: 3165728

6

Deletions of the steroid sulphatase gene in "classical" X-linked ichthyosis and in X-linked ichthyosis associated with Kallmann syndrome.

Ballabio A, Sebastio G, Carrozzo R, Parenti G, Piccirillo A, Persico MG, Andria G. Ballabio A, et al. Among authors: parenti g. Hum Genet. 1987 Dec;77(4):338-41. doi: 10.1007/BF00291422. Hum Genet. 1987. PMID: 3480263

7

Immunological disorder and Hirschsprung disease in round femoral inferior epiphysis dysplasia.

Lecora M, Parenti G, Iaccarino E, Scarano G, Cucchiara S, Andria G. Lecora M, et al. Among authors: parenti g. Clin Dysmorphol. 1995 Apr;4(2):130-5. Clin Dysmorphol. 1995. PMID: 7606319

8

Variable penetrance of hypogonadism in a sibship with Kallmann syndrome due to a deletion of the KAL gene.

Parenti G, Rizzolo MG, Ghezzi M, Di Maio S, Sperandeo MP, Incerti B, Franco B, Ballabio A, Andria G. Parenti G, et al. Am J Med Genet. 1995 Jul 3;57(3):476-8. doi: 10.1002/ajmg.1320570323. Am J Med Genet. 1995. PMID: 7677154

9

Lysinuric protein intolerance characterized by bone marrow abnormalities and severe clinical course.

Parenti G, Sebastio G, Strisciuglio P, Incerti B, Pecoraro C, Terracciano L, Andria G. Parenti G, et al. J Pediatr. 1995 Feb;126(2):246-51. doi: 10.1016/s0022-3476(95)70552-x. J Pediatr. 1995. PMID: 7844671 Review.

10

Early detection of lung involvement in lysinuric protein intolerance: role of high-resolution computed tomography and radioisotopic methods.

Santamaria F, Parenti G, Guidi G, Rotondo A, Grillo G, Larocca MR, Celentano L, Strisciuglio P, Sebastio G, Andria G. Santamaria F, et al. Among authors: parenti g. Am J Respir Crit Care Med. 1996 Feb;153(2):731-5. doi: 10.1164/ajrccm.153.2.8564125. Am J Respir Crit Care Med. 1996. PMID: 8564125

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