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Klinika pediatryczna nr 2021 - neurometabolizm
12307637
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Description
- Fenotyp chorób mitochondrialnych – od zespołu Leigha do encefalopatii
- Rdzeniowy zanik mięśni – metody i efekty leczenia
- Leczenie dietetyczne chorób rzadkich z uwzględnieniem leczenia żywieniowego
- Dieta bogatotłuszczowa we wrodzonych chorobach metabolicznych – nowe wskazania
- Praktyczne aspekty poradnictwa genetycznego we wrodzonych błędach metabolizmu
- Wybrane przyczyny hiperamonemii
- Patofizjologia hiperamonemii
- Nowe perspektywy w leczeniu glikogenozy typu Ia
- Nowe perspektywy w leczeniu glikogenozy 1b
- Niedobór kobalaminy i zaburzenia jej przemian
- Nowoczesne podejście do roli fizjoterapeuty w leczeniu dzieci z hemofilią A i B
- Ciągłość opieki nad pacjentem z rzadką chorobą metaboliczną, czy tylko problem internistyczny?
- Choroby rzadkie – perspektywa pacjentów i opiekunów
- Pacjenci z chorobą Huntera (mukopolisacharydozą typu II) leczeni enzymatyczną terapią zastępczą z wczesnym i późnym początkiem leczenia (aktualizacja dla pacjenta 1 i 2:: lata 2018-2020)
Product Details
17897
1230-7637
Data sheet
- Published in
- Warszawa
- Publication date
- 2021
- Issue number
- 1
- Cover
- soft
- Pages count
- 70
- Dimensions (mm)
- 210 x 295
- Weight (g)
- 240
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