Creato da XagenaMedicina il 15/10/2009

Xagena Medicina

Discussione di argomenti medico-farmacologici

Messaggi del 02/07/2014

Dermatology News by Xagena

DermatologyNews.net - Dermatology
Dermatology, DermatologyNews.net - Dermatology Xagena, Xagena Medical News, Eczema, Melanoma, Dermatitis, Rosacea, Psoriasis, Skin diseases, Skin drugs
 
Dermatology Xagena
Raptiva ( Efalizumab) is indicated for the treatment of adult ...
Eczema
Eczema: Elidel and Protopic should be used cautiously. The ...
Raptiva
Raptiva ( Efalizumab) is indicated for the treatment of adult ...
Lambrolizumab shows ...
Lambrolizumab shows promise for treating metastatic melanoma ...
Nivolumab
Nivolumab with vaccine in Ipilimumab-refractory or -naive ...
Eczema: Elidel and Protopic ...
Eczema: Elidel and Protopic should be used cautiously. The ...
DermatologyNews.net ...
DermatologyNews.net - Dermatology Xagena · Home ...
Skin cancer and lymphoma n ...
Skin cancer and lymphoma n patients treated with ...
Aldara for the treatment of ...
Aldara for the treatment of actinic keratosis. The 5% Imiquimod ...
Skin infection
Antimicrobial gene prevents skin infection. Bacterial resistance to ...

 
 
 

Rare diseases by Xagena

RareDiseasesNews.net - Rare disease
Rare diseases, Orphan drugs, Rare disease, Rare disease Xagena, Xagena Medical News, Rare syndrome, Rare neurological disorders, Orphan drug,
 
RareDiseasesNews.net - Rare ...
RareDiseasesNews.net - Rare diseases Xagena ... Late-onset ...
Rett syndrome
Rett syndrome is a neurodevelopmental disorder ...
Plerixafor targets specific ...
Plerixafor targets specific defect causing WHIM syndrome. A ...
Alagille syndrome
NOTCH2 mutations gene found for Alagille syndrome may be ...
Bronchiectasis
FDA OOPD: orphan drug designation for Erdosteine in ...
Vitamin B12 deficiency
Discovered a mutation that causes a rare, inherited vitamin B12 ...
Fanconi anemia
Fanconi anemia ( FA ) is a rare genetic disorder which affects ...
Hepatic porphyria
Variegate porphyria ( VP ) is an autosomal dominantly inherited ...
Prader-Willi syndrome
Prader-Willi syndrome is a rare genetic disorder which affects ...
Aplastic anemia
A comparison clinical study of two aplastic anemia treatments ...

 
 
 
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