171 related articles for article (PubMed ID: 24898502)
1. [Rare diseases are common].
Has C; Giehl K
Hautarzt; 2014 Jun; 65(6):488-9. PubMed ID: 24898502
[No Abstract] [Full Text] [Related]
2. [Genodermatoses with malignant skin tumors].
Hübinger L; Frank J
Hautarzt; 2014 Jun; 65(6):527-35. PubMed ID: 24898507
[TBL] [Abstract][Full Text] [Related]
3. A multistep approach to the diagnosis of rare genodermatoses.
Tantcheva-Poór I; Oji V; Has C
J Dtsch Dermatol Ges; 2016 Oct; 14(10):969-986. PubMed ID: 27767270
[TBL] [Abstract][Full Text] [Related]
4. [How frequently does genetic mosaicism occur in the skin?].
Happle R
Hautarzt; 2014 Jun; 65(6):536-41. PubMed ID: 24898508
[TBL] [Abstract][Full Text] [Related]
5. [Alopecia and hypotrichosis in childhood: clinical features and diagnosis].
Betz RC
Hautarzt; 2014 Jun; 65(6):520-6. PubMed ID: 24898506
[TBL] [Abstract][Full Text] [Related]
6. [Practical aspects of molecular diagnostics in genodermatoses].
Has C; He Y
Hautarzt; 2016 Jan; 67(1):53-8. PubMed ID: 26537890
[TBL] [Abstract][Full Text] [Related]
7. Vulvar Dyschromia in a Child: A Quiz.
de Lorenzi C; Kaya G; Quenan S; Calza AM
Acta Derm Venereol; 2019 Jun; 99(7):711-712. PubMed ID: 30938832
[No Abstract] [Full Text] [Related]
8. Generalized Skin Scaling in a Young Girl: A Quiz.
Mo R; Wang H; Lin Z
Acta Derm Venereol; 2019 Dec; 99(13):1322-1323. PubMed ID: 31612237
[No Abstract] [Full Text] [Related]
9. 23andMe resumes giving consumers genetic health information: Company's tests for rare and common diseases aren't diagnostic.
Am J Med Genet A; 2017 Aug; 173(8):2003-2004. PubMed ID: 28703454
[No Abstract] [Full Text] [Related]
10. [Ophthalmogenetics: Rare Diseases - A Challenge for Diagnostic and Treatment].
Rudolph G
Klin Monbl Augenheilkd; 2016 Mar; 232(3):242. PubMed ID: 27011027
[No Abstract] [Full Text] [Related]
11. Adopting orphans: comprehensive genetic testing of Mendelian diseases of childhood by next-generation sequencing.
Kingsmore SF; Dinwiddie DL; Miller NA; Soden SE; Saunders CJ
Expert Rev Mol Diagn; 2011 Nov; 11(8):855-68. PubMed ID: 22022947
[TBL] [Abstract][Full Text] [Related]
12. Phen-Gen: combining phenotype and genotype to analyze rare disorders.
Javed A; Agrawal S; Ng PC
Nat Methods; 2014 Sep; 11(9):935-7. PubMed ID: 25086502
[TBL] [Abstract][Full Text] [Related]
13. [Genodermatoses].
Frank J
Hautarzt; 2004 Oct; 55(10):919. PubMed ID: 15635734
[No Abstract] [Full Text] [Related]
14. Rare conditions: where do primary care and genetic diseases intersect?
Terry SF; Krokosky A
JAAPA; 2010 Nov; 23(11):63-4. PubMed ID: 21086896
[No Abstract] [Full Text] [Related]
15. Painful subcutaneous nodules in a patient with shortened digits.
Johnson BC; Morrell DS
Pediatr Dermatol; 2019 Nov; 36(6):944-945. PubMed ID: 31778566
[No Abstract] [Full Text] [Related]
16. Ligneous conjunctivitis in a young patient with homozygous K19E plasminogen gene mutation: a diagnostic and therapeutic challenge.
Kuonen A; Vaudaux J; Hamedani M; Schuster V; Albisetti M; von der Weid N; Kaeser PF
Klin Monbl Augenheilkd; 2013 Apr; 230(4):346-8. PubMed ID: 23629776
[No Abstract] [Full Text] [Related]
17. Next Generation Diagnostics for Rare Neurological Diseases: The Future is Here.
Innes AM; Boycott KM
Can J Neurol Sci; 2014 May; 41(3):299-300. PubMed ID: 24718813
[No Abstract] [Full Text] [Related]
18. Ending a Diagnostic Odyssey: Family Education, Counseling, and Response to Eventual Diagnosis.
Basel D; McCarrier J
Pediatr Clin North Am; 2017 Feb; 64(1):265-272. PubMed ID: 27894449
[TBL] [Abstract][Full Text] [Related]
19. A multistep approach to the diagnosis of rare genodermatoses.
Aşkın Ö; Engin B; Gencebay G; Tüzün Y
Clin Dermatol; 2020; 38(4):399-407. PubMed ID: 32972599
[TBL] [Abstract][Full Text] [Related]
20. The Molecular Revolution in Cutaneous Biology: Era of Molecular Diagnostics for Inherited Skin Diseases.
McGrath JA
J Invest Dermatol; 2017 May; 137(5):e83-e86. PubMed ID: 28411852
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]