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Klinika pediatryczna nr 2019 - neurometabolizm
12307637
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Description
- METABOLIZM
Diagnostyka i leczenie ostrej hiperamonemii - rola kwasu kargluminowego
Tyrozynemia typ I - podstawy diagnostyki i leczenia
Dystrofia mięśniowa Duchennea/Beckera - diagnostyka molekularna
Dystrofia mięśniowa typu Duchennea (DMD) - od objawów do rozpoznania
Opieka endokrynologiczna u pacjentów z dystrofią mięśniową Duchennea
Powikłania pulmonologiczne u pacjentów z dystrofią mięśniową typu Duchennea
Problemy gastroenterologiczne pacjentów z dystrofią mięśniową typu Duchennea
Spektrum problemów kardiologicznych w dystrofiach mięśniowych. Historia naturalna, diagnostyka i leczenie.
Zalecenia żywieniowe dla pacjentów z dystrofią mięśniową typu Duchennea
Czym różni się choroba Morquio (mukopolisacharydoza typu IV A) od pozostałych typów mukopolisacharydoz?
Pacjenci z chorobą Huntera (mukopolisacharydozą typu II) leczeni enzymatyczną terapią zastępczą
Pacjenci z chorobą Hurler/Scheie
GOSPODARKA WAPNIOWO-FOSFORANOWA
Rzadkie przyczyny hiperkalcemii u dzieci
Rodzinna krzywica hipofosfatemiczna
CHOROBY NEREK
Uwarunkowane genetycznie tubulopatie - diagnostyka i leczenie
Rzadkie wrodzone choroby nerek
GENETYKA
Diagnostyka prenatalna - nowe wyzwania
Niepełnosprawność intelektualna uwarunkowana genetycznie
Ultrasonograficzne badanie przezciemiączkowe w diagnostyce wrodzonych chorób neurometabolicznych
CHOROBY UKŁADU KOSTNEGO
Osteoporoza u dzieci
Wrodzona łamliwość kości u noworodków
Product Details
16287
1230-7637
Data sheet
- Published in
- Warszawa
- Publication date
- 2019
- Issue number
- 1
- Cover
- soft
- Pages count
- 116
- Dimensions (mm)
- 210 x 295
- Weight (g)
- 410
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