Finsterer J, Fellinger J

Idioma: Ingles.
Referencias bibliográficas: 9
Paginas: 322-324
Archivo PDF: 143.41 Kb.

FRAGMENTO

Sin resumen

REFERENCIAS (EN ESTE ARTÍCULO)

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2. Brisson D, Houde G, St-Pierre J, Vohl MC, Mathieu J, Gaudet D. The pleiotropic expression of the myotonic dystrophy protein kinase gene illustrates the complex relationships between genetic, biological and clinical covariates of male aging. Aging Male 2002; 5: 223-32.

3. Wheeler TM, Thornton CA. Myotonic dystrophy: RNA-mediated muscle disease. Curr Opin Neurol 2007; 20: 572-6.

4. Wheeler TM. Myotonic dystrophy: therapeutic strategies for the future. Neurotherapeutics 2008; 5: 592-600.

5. Inui S, Note S, Aoyama I, Tokimitsu N, Matsutomo K. 3 cases of dystrophia myotonica in a sister, brother and cousin. Nippon Rinsho 1968; 26: 1928-32.

6. Cooper SM, Dawber RP, Hilton-Jones D. Three cases of androgen- dependent disease associated with myotonic dystrophy. J Eur Acad Dermatol Venereol 2003; 17: 56-8.

7. Mounsey AL, Reed SW. Diagnosing and treating hair loss. Am Fam Physician 2009; 80: 356-62.

8. Itin PH, Laeng RH. Multiple pigmented basalioma of the scalp in a patient with Curschmann-Steinert myotonia dystrophica. Confirmation of a rare symptom constellation. Hautarzt 2001; 52: 244-6.

9. Ravindra BS, Desai N, Deviprasad S, Bhede V, Ravat S, Sawant P. Myotonic dystrophy in a patient of celiac disease: a new association? Trop Gastroenterol 2008; 29: 114-5.