Raghunath M - Search Results

1

[Marfan syndrome: prevalence and natural course of cardiovascular manifestations].

von Kodolitsch Y, Raghunath M, Nienaber CA. von Kodolitsch Y, et al. Among authors: raghunath m. Z Kardiol. 1998 Mar;87(3):150-60. doi: 10.1007/s003920050167. Z Kardiol. 1998. PMID: 9586150 Review. German.

2

[Marfan syndrome: strategies of interdisciplinary care].

von Kodolitsch Y, Raghunath M, Nienaber CA. von Kodolitsch Y, et al. Among authors: raghunath m. Dtsch Med Wochenschr. 1998 Jan 2;123(1-2):21-5. doi: 10.1055/s-2007-1023893. Dtsch Med Wochenschr. 1998. PMID: 9465852 Review. German. No abstract available.

3

[Marfan syndrome: diagnosis of cardiovascular manifestations].

von Kodolitsch Y, Raghunath M, Dieckmann C, Nienaber CA. von Kodolitsch Y, et al. Among authors: raghunath m. Z Kardiol. 1998 Mar;87(3):161-72. doi: 10.1007/s003920050168. Z Kardiol. 1998. PMID: 9586151 Review. German.

4

[Marfan syndrome: therapy of cardiovascular manifestations].

von Kodolitsch Y, Raghunath M, Karck M, Haverich A, Nienaber CA. von Kodolitsch Y, et al. Among authors: raghunath m. Z Kardiol. 1998 Mar;87(3):173-84. doi: 10.1007/s003920050169. Z Kardiol. 1998. PMID: 9586152 Review. German.

5

Ehlers-Danlos Syndrome Type VI (EDS VI): problems of diagnosis and management.

Heim P, Raghunath M, Meiss L, Heise U, Myllylä R, Kohlschütter A, Steinmann B. Heim P, et al. Among authors: raghunath m. Acta Paediatr. 1998 Jun;87(6):708-10. doi: 10.1080/080352598750014184. Acta Paediatr. 1998. PMID: 9686670

6

A point mutation creating an extra N-glycosylation site in fibrillin-1 results in neonatal Marfan syndrome.

Lönnqvist L, Karttunen L, Rantamäki T, Kielty C, Raghunath M, Peltonen L. Lönnqvist L, et al. Among authors: raghunath m. Genomics. 1996 Sep 15;36(3):468-75. doi: 10.1006/geno.1996.0492. Genomics. 1996. PMID: 8884270

7

Prenatal diagnosis of Marfan syndrome: identification of a fibrillin-1 mutation in chorionic villus sample.

Rantamäki T, Raghunath M, Karttunen L, Lönnqvist L, Child A, Peltonen L. Rantamäki T, et al. Among authors: raghunath m. Prenat Diagn. 1995 Dec;15(12):1176-81. doi: 10.1002/pd.1970151217. Prenat Diagn. 1995. PMID: 8750301

8

Abnormal morphology of fibrillin microfibrils in fibroblast cultures from patients with neonatal Marfan syndrome.

Godfrey M, Raghunath M, Cisler J, Bevins CL, DePaepe A, Di Rocco M, Gregoritch J, Imaizumi K, Kaplan P, Kuroki Y, et al. Godfrey M, et al. Among authors: raghunath m. Am J Pathol. 1995 Jun;146(6):1414-21. Am J Pathol. 1995. PMID: 7778680 Free PMC article.

9

Decreased extracellular deposition of fibrillin and decorin in neonatal Marfan syndrome fibroblasts.

Raghunath M, Superti-Furga A, Godfrey M, Steinmann B. Raghunath M, et al. Hum Genet. 1993 Jan;90(5):511-5. doi: 10.1007/BF00217450. Hum Genet. 1993. PMID: 8428751

10

Deficiencies of fibrillin and decorin in fibroblast cultures of a patient with neonatal Marfan syndrome.

Superti-Furga A, Raghunath M, Willems PJ. Superti-Furga A, et al. Among authors: raghunath m. J Med Genet. 1992 Dec;29(12):875-8. doi: 10.1136/jmg.29.12.875. J Med Genet. 1992. PMID: 1479602 Free PMC article.

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