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Identyfikacja mutacji w mitochondrialnym genie 12S rRNA u osób z niedosłuchem po leczeniu antybiotykami aminoglikozydowymi
Identyfikacja mutacji w mitochondrialnym genie 12S rRNA u osób z niedosłuchem po leczeniu antybiotykami aminoglikozydowymi
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Identyfikacja mutacji w mitochondrialnym genie 12S rRNA u osób z niedosłuchem po leczeniu antybiotykami aminoglikozydowymi

Rydzanicz, Małgorzata

Otolaryngologia Polska, 2011-07, Vol.65 (4), p.297-299 [Periódico revisado por pares]

Elsevier Urban & Partner (Poland)

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2
Mutational screening of the mitochondrial 12S rRNA gene in Polish patients with aminoglycoside-induced hearing loss
Mutational screening of the mitochondrial 12S rRNA gene in Polish patients with aminoglycoside-induced hearing loss
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Mutational screening of the mitochondrial 12S rRNA gene in Polish patients with aminoglycoside-induced hearing loss

Rydzanicz, Małgorzata

Otolaryngologia Polska, 2011-07, Vol.65 (4), p.297-299 [Periódico revisado por pares]

Poland

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3
The role of skeletal muscle biopsy in the diagnosis of neuromuscular disorders
The role of skeletal muscle biopsy in the diagnosis of neuromuscular disorders
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The role of skeletal muscle biopsy in the diagnosis of neuromuscular disorders

Nadaj-Pakleza, Aleksandra ; Kierdaszuk, Biruta ; Kamińska, Anna

Neurologia i neurochirurgia polska, 2010-09, Vol.44 (5), p.481-491 [Periódico revisado por pares]

Kraków: Wydawnictwo Via Medica

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4
The molecular background of Leigh syndrome
The molecular background of Leigh syndrome
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The molecular background of Leigh syndrome

Piekutowska-Abramczuk, Dorota

Neurologia i neurochirurgia polska, 2008-05, Vol.42 (3), p.238-250 [Periódico revisado por pares]

Poland

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5
Mutacje mitochondrialnego DNA w rozwoju nowotworów głowy i szyi
Mutacje mitochondrialnego DNA w rozwoju nowotworów głowy i szyi
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Mutacje mitochondrialnego DNA w rozwoju nowotworów głowy i szyi

Piętka, Grzegorz ; Kukwa, Wojciech ; Bartnik, Ewa ; Ścińska, Anna ; Czarnecka, Anna M.

Otolaryngologia Polska, 2008, Vol.62 (2), p.158-164 [Periódico revisado por pares]

Elsevier Sp. z o.o

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6
Mitochondrial DNA mutations in the pathogenesis in the head and neck squamous cell carcinoma
Mitochondrial DNA mutations in the pathogenesis in the head and neck squamous cell carcinoma
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Mitochondrial DNA mutations in the pathogenesis in the head and neck squamous cell carcinoma

Pietka, Grzegorz ; Kukwa, Wojciech ; Bartnik, Ewa ; Scińska, Anna ; Czarnecka, Anna M

Otolaryngologia Polska, 2008, Vol.62 (2), p.158 [Periódico revisado por pares]

Poland

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7
Mutations in the mitofusin 2 gene are the most common cause of Charcot-Marie-Tooth type 2 disease
Mutations in the mitofusin 2 gene are the most common cause of Charcot-Marie-Tooth type 2 disease
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Mutations in the mitofusin 2 gene are the most common cause of Charcot-Marie-Tooth type 2 disease

Sołtysińska, Ewa ; Kabzińska, Dagmara ; Kochański, Andrzej

Neurologia i neurochirurgia polska, 2007-07, Vol.41 (4), p.350-354 [Periódico revisado por pares]

Poland

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8
Leber's hereditary optic neuropathy (LHON) with mutation at G3460A and MS-like phenotype
Leber's hereditary optic neuropathy (LHON) with mutation at G3460A and MS-like phenotype
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Leber's hereditary optic neuropathy (LHON) with mutation at G3460A and MS-like phenotype

Jamrozik, Zygmunt ; Tutaj, Andrzej ; Piechowski-Jóźwiak, Bartłomiej ; Mroczek-Tońska, Katarzyna ; Bartnik, Ewa ; Kwieciński, Hubert

Neurologia i neurochirurgia polska, 2003-05, Vol.37 (3), p.713-720 [Periódico revisado por pares]

Poland

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9
A case or Leber hereditary optic neuropathy (LHON): differential diagnosis with post inflammatory atrophy of nerve II using the mtDNA analysis
A case or Leber hereditary optic neuropathy (LHON): differential diagnosis with post inflammatory atrophy of nerve II using the mtDNA analysis
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A case or Leber hereditary optic neuropathy (LHON): differential diagnosis with post inflammatory atrophy of nerve II using the mtDNA analysis

Lubos, Leszek ; Wajgt, Andrzej ; Maciejowski, Maciej ; Mroczek-Tońska, Katarzyna ; Bartnik, Ewa ; Dziekanowska, Danuta

Neurologia i neurochirurgia polska, 2003-01, Vol.37 (1), p.229-234 [Periódico revisado por pares]

Poland

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10
MELAS--mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes syndrome--two cases confirmed by biochemical and molecular investigations. Differential diagnosis of stroke causes
MELAS--mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes syndrome--two cases confirmed by biochemical and molecular investigations. Differential diagnosis of stroke causes
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MELAS--mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes syndrome--two cases confirmed by biochemical and molecular investigations. Differential diagnosis of stroke causes

Mierzewska, Hanna ; Mroczek, Katarzyna ; Pronicki, Maciej ; Pronicka, Ewa ; Karczmarewicz, Elzbieta ; Bartnik, Ewa ; Zdzienicka, Elzbieta ; Seniów, Joanna ; Schmidt-Sidor, Bogna ; Taraszewska, Anna ; Palasik, Witold

Neurologia i neurochirurgia polska, 2002-05, Vol.36 (3), p.457-470 [Periódico revisado por pares]

Poland

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