תסמונת מרף (Hebrew Wikipedia)

Analysis of information sources in references of the Wikipedia article "תסמונת מרף" in Hebrew language version.

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ama-assn.org

Melone MA, Tessa A, Petrini S (בפברואר 2004). "Revelation of a new mitochondrial DNA mutation (G12147A) in a MELAS/MERFF phenotype". Arch. Neurol. 61 (2): 269–72. doi:10.1001/archneur.61.2.269. PMID 14967777. {{cite journal}}: (עזרה)תחזוקה - ציטוט: multiple names: authors list (link)(הקישור אינו פעיל)

Melone MA, Tessa A, Petrini S (בפברואר 2004). "Revelation of a new mitochondrial DNA mutation (G12147A) in a MELAS/MERFF phenotype". Arch. Neurol. 61 (2): 269–72. doi:10.1001/archneur.61.2.269. PMID 14967777. {{cite journal}}: (עזרה)תחזוקה - ציטוט: multiple names: authors list (link)(הקישור אינו פעיל)
Nakamura M, Nakano S, Goto Y (בספטמבר 1995). "A novel point mutation in the mitochondrial tRNA(Ser(UCN)) gene detected in a family with MERRF/MELAS overlap syndrome". Biochem. Biophys. Res. Commun. 214 (1): 86–93. doi:10.1006/bbrc.1995.2260. PMID 7669057. {{cite journal}}: (עזרה)תחזוקה - ציטוט: multiple names: authors list (link)

Nakamura M, Nakano S, Goto Y (בספטמבר 1995). "A novel point mutation in the mitochondrial tRNA(Ser(UCN)) gene detected in a family with MERRF/MELAS overlap syndrome". Biochem. Biophys. Res. Commun. 214 (1): 86–93. doi:10.1006/bbrc.1995.2260. PMID 7669057. {{cite journal}}: (עזרה)תחזוקה - ציטוט: multiple names: authors list (link)

Mancuso M, Filosto M, Mootha VK (ביוני 2004). "A novel mitochondrial tRNAPhe mutation causes MERRF syndrome". Neurology. 62 (11): 2119–21. PMID 15184630. {{cite journal}}: (עזרה)תחזוקה - ציטוט: multiple names: authors list (link)

Zeviani M, Muntoni F, Savarese N (1993). "A MERRF/MELAS overlap syndrome associated with a new point mutation in the mitochondrial DNA tRNA(Lys) gene". Eur. J. Hum. Genet. 1 (1): 80–7. PMID 8069654.{{cite journal}}: תחזוקה - ציטוט: multiple names: authors list (link)
Melone MA, Tessa A, Petrini S (בפברואר 2004). "Revelation of a new mitochondrial DNA mutation (G12147A) in a MELAS/MERFF phenotype". Arch. Neurol. 61 (2): 269–72. doi:10.1001/archneur.61.2.269. PMID 14967777. {{cite journal}}: (עזרה)תחזוקה - ציטוט: multiple names: authors list (link)(הקישור אינו פעיל)
Nakamura M, Nakano S, Goto Y (בספטמבר 1995). "A novel point mutation in the mitochondrial tRNA(Ser(UCN)) gene detected in a family with MERRF/MELAS overlap syndrome". Biochem. Biophys. Res. Commun. 214 (1): 86–93. doi:10.1006/bbrc.1995.2260. PMID 7669057. {{cite journal}}: (עזרה)תחזוקה - ציטוט: multiple names: authors list (link)
Mancuso M, Filosto M, Mootha VK (ביוני 2004). "A novel mitochondrial tRNAPhe mutation causes MERRF syndrome". Neurology. 62 (11): 2119–21. PMID 15184630. {{cite journal}}: (עזרה)תחזוקה - ציטוט: multiple names: authors list (link)