Melotti D - Search Results

1

Cytomegalovirus DNA detection in Guthrie cards: a powerful tool for diagnosing congenital infection.

Barbi M, Binda S, Primache V, Caroppo S, Didò P, Guidotti P, Corbetta C, Melotti D. Barbi M, et al. Among authors: melotti d. J Clin Virol. 2000 Sep 1;17(3):159-65. doi: 10.1016/s1386-6532(00)00089-5. J Clin Virol. 2000. PMID: 10996112

2

CMV gB genotypes and outcome of vertical transmission: study on dried blood spots of congenitally infected babies.

Barbi M, Binda S, Caroppo S, Primache V, Didò P, Guidotti P, Corbetta C, Melotti D. Barbi M, et al. Among authors: melotti d. J Clin Virol. 2001 Apr;21(1):75-9. doi: 10.1016/s1386-6532(00)00188-8. J Clin Virol. 2001. PMID: 11255100

3

Palmoplantar keratoderma of Unna-Thost: response to biotin in one family.

Menni S, Saleh F, Piccinno R, Corbetta C, Melotti D. Menni S, et al. Among authors: melotti d. Clin Exp Dermatol. 1992 Sep;17(5):337-8. doi: 10.1111/j.1365-2230.1992.tb00224.x. Clin Exp Dermatol. 1992. PMID: 1458638 No abstract available.

4

A difficult diagnosis of lysinuric protein intolerance: association with glucose-6-phosphate dehydrogenase deficiency.

Parini R, Vegni M, Pontiggia M, Melotti D, Corbetta C, Rossi A, Piceni Sereni L. Parini R, et al. Among authors: melotti d. J Inherit Metab Dis. 1991;14(5):833-4. doi: 10.1007/BF01799959. J Inherit Metab Dis. 1991. PMID: 1779632 No abstract available.

5

Medium-chain triglyceride loading test in carnitine-acylcarnitine translocase deficiency: insights on treatment.

Parini R, Invernizzi F, Menni F, Garavaglia B, Melotti D, Rimoldi M, Salera S, Tosetto C, Taroni F. Parini R, et al. Among authors: melotti d. J Inherit Metab Dis. 1999 Aug;22(6):733-9. doi: 10.1023/a:1005548201355. J Inherit Metab Dis. 1999. PMID: 10472533

6

Clinical diagnosis of long-chain acyl-coenzyme A-dehydrogenase deficiency: use of stress and fat-loading tests.

Parini R, Garavaglia B, Saudubray JM, Bardelli P, Melotti D, Zecca G, Di Donato S. Parini R, et al. Among authors: melotti d. J Pediatr. 1991 Jul;119(1 Pt 1):77-80. doi: 10.1016/s0022-3476(05)81044-3. J Pediatr. 1991. PMID: 2066862 No abstract available.

7

Acute, severe cardiomyopathy as main symptom of late-onset very long-chain acyl-coenzyme A dehydrogenase deficiency.

Parini R, Menni F, Garavaglia B, Fesslova V, Melotti D, Massone ML, Lamantea E, Rimoldi M, Vizziello P, Gatti R. Parini R, et al. Among authors: melotti d. Eur J Pediatr. 1998 Dec;157(12):992-5. doi: 10.1007/s004310050984. Eur J Pediatr. 1998. PMID: 9877038

8

Age, menopausal status and homocysteine levels in women around menopause.

Bruschi F, Daguati R, Parazzini F, Dal Pino D, Fiore V, Di Pace R, Melotti D, Moroni S, Maffioletti C, Rossi M, Crosignani PG. Bruschi F, et al. Among authors: melotti d. Eur J Obstet Gynecol Reprod Biol. 2005 Jun 1;120(2):195-7. doi: 10.1016/j.ejogrb.2004.11.016. Eur J Obstet Gynecol Reprod Biol. 2005. PMID: 15925051

9

Effect of oral or transdermal hormone replacement therapy on homocysteine levels: a randomized clinical trial.

Bruschi F, Dal Pino D, Fiore V, Parazzini F, Di Pace R, Cesana BM, Melotti D, Crosignani PG. Bruschi F, et al. Among authors: melotti d. Maturitas. 2004 May 28;48(1):33-8. doi: 10.1016/j.maturitas.2003.08.005. Maturitas. 2004. PMID: 15223106 Clinical Trial.

10

Newborn screening of homocystinuria: quantitative analysis of total homocyst(e)ine on dried blood spot by liquid chromatography with fluorimetric detection.

Accinni R, Campolo J, Parolini M, De Maria R, Caruso R, Maiorana A, Galluzzo C, Bartesaghi S, Melotti D, Parodi O. Accinni R, et al. Among authors: melotti d. J Chromatogr B Analyt Technol Biomed Life Sci. 2003 Mar 5;785(2):219-26. doi: 10.1016/s1570-0232(02)00852-8. J Chromatogr B Analyt Technol Biomed Life Sci. 2003. PMID: 12554134

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