Results 311 to 320 of about 1,030,121 (356)
Some of the next articles are maybe not open access.
2012
Chediak-Higashi Disease – Chronic Granulomatous Disease – Epidermodysplasia Verruciformis – Familial Mucocutaneous Candidiasis – Griscelli Syndrome Types 1 and 2 – Job Syndrome – Mucoepithelial Dysplasia – Wiskott-Aldrich ...
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Chediak-Higashi Disease – Chronic Granulomatous Disease – Epidermodysplasia Verruciformis – Familial Mucocutaneous Candidiasis – Griscelli Syndrome Types 1 and 2 – Job Syndrome – Mucoepithelial Dysplasia – Wiskott-Aldrich ...
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1999
Just over 25 years ago, De Weerdt and Castelain [1] described the combination of progressive muscular weakness and dystrophic epidermolysis bullosa with an autosomal recessive pattern. Niemi et al. [2] described a Finnish sibship with normal parents and 12 members.
Josanne Aquilina +4 more
openaire +2 more sources
Just over 25 years ago, De Weerdt and Castelain [1] described the combination of progressive muscular weakness and dystrophic epidermolysis bullosa with an autosomal recessive pattern. Niemi et al. [2] described a Finnish sibship with normal parents and 12 members.
Josanne Aquilina +4 more
openaire +2 more sources
Carbohydrate Deficiency Diseases
1997Recent refinements in carbohydrate analytical methodology and the application of molecular cloning techniques have defined a whole new area of carbohydrate pathology. Several forms of carbohydrate deficiency diseases have been described. These relate to impairment of glycoprotein processing or biosynthesis.
William Kuhns, Inka Brockhausen
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The Immunological Deficiency Diseases
Medical Clinics of North America, 1970Richard A. Gatti +2 more
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Poly(ADP-Ribose) polymerase (PARP) inhibitors: Exploiting a synthetic lethal strategy in the clinic
Ca-A Cancer Journal for Clinicians, 2011Timothy A Yap, Johann S De Bono
exaly