Ebrahimi-Fakhari D - Search Results

1

[Non-ambulatory patients with Duchenne muscular dystrophy : Recommendations for monitoring disease progression and course of treatment].

Flotats-Bastardas M, Ebrahimi-Fakhari D, Bernert G, Ziegler A, Schlachter K, Poryo M, Hahn A, Meyer S. Flotats-Bastardas M, et al. Nervenarzt. 2019 Aug;90(8):817-823. doi: 10.1007/s00115-019-0754-y. Nervenarzt. 2019. PMID: 31270551 Review. German.

2

[ESPED-Survey: TSC-disease in children and adolescents: preliminary results from a German epidemiological survey].

Mann L, Ebrahimi-Fakhari D, Heinrich B, Flotats-Bastardas M, Gortner L, von Gontard A, Niemcyzk J, Poryo M, Meyer S. Mann L, et al. Wien Med Wochenschr. 2017 Sep;167(11-12):271-275. doi: 10.1007/s10354-016-0522-6. Epub 2016 Nov 3. Wien Med Wochenschr. 2017. PMID: 27812765 German.

3

Topical Rapamycin for Facial Angiofibromas in a Child with Tuberous Sclerosis Complex (TSC): A Case Report and Long-Term Follow-up.

Ebrahimi-Fakhari D, Müller CSL, Meyer S, Flotats-Bastardas M, Vogt T, Pföhler C. Ebrahimi-Fakhari D, et al. Dermatol Ther (Heidelb). 2017 Mar;7(1):175-179. doi: 10.1007/s13555-017-0174-5. Epub 2017 Feb 8. Dermatol Ther (Heidelb). 2017. PMID: 28181194 Free PMC article.

4

Dermatological manifestations of tuberous sclerosis complex (TSC).

Ebrahimi-Fakhari D, Meyer S, Vogt T, Pföhler C, Müller CSL. Ebrahimi-Fakhari D, et al. J Dtsch Dermatol Ges. 2017 Jul;15(7):695-700. doi: 10.1111/ddg.13264. Epub 2017 Jun 9. J Dtsch Dermatol Ges. 2017. PMID: 28598544 Review.

5

Dermatologische Manifestationen der tuberösen Sklerose (TSC).

Ebrahimi-Fakhari D, Meyer S, Vogt T, Pföhler C, Müller CSL. Ebrahimi-Fakhari D, et al. J Dtsch Dermatol Ges. 2017 Jul;15(7):695-701. doi: 10.1111/ddg.13264_g. J Dtsch Dermatol Ges. 2017. PMID: 28677177 Review. No abstract available.

6

Ante-, peri- and postnatal factors associated with intraventricular hemorrhage in very premature infants.

Poryo M, Boeckh JC, Gortner L, Zemlin M, Duppré P, Ebrahimi-Fakhari D, Wagenpfeil S, Heckmann M, Mildenberger E, Hilgendorff A, Flemmer AW, Frey G, Meyer S; PROGRESS study consortium and NGFN - Nationales Genomforschungsnetz Deutschland. Poryo M, et al. Early Hum Dev. 2018 Jan;116:1-8. doi: 10.1016/j.earlhumdev.2017.08.010. Epub 2017 Nov 5. Early Hum Dev. 2018. PMID: 29091782

7

Optimized care in Patients with Rare Diseases: TSC at the Center for Rare Diseases (ZSEUKS) at Saarland University Medical Center, Germany.

Ebrahimi-Fakhari D, Poryo M, Graf N, Zemlin M, Flotats-Bastardas M, Heine G, Ragoschke-Schumm A, Meyer S. Ebrahimi-Fakhari D, et al. Klin Padiatr. 2017 Nov;229(6):311-315. doi: 10.1055/s-0043-120069. Epub 2017 Nov 13. Klin Padiatr. 2017. PMID: 29132163 Review. English.

8

Diagnosis and Treatment of Tuberous Sclerosis Manifestations in Children: A Multicenter Study.

Flotats-Bastardas M, Ebrahimi-Fakhari D, Gortner L, Poryo M, Zemlin M, Macaya-Ruiz A, Meyer S. Flotats-Bastardas M, et al. Neuropediatrics. 2018 Jun;49(3):193-199. doi: 10.1055/s-0038-1637738. Epub 2018 Mar 20. Neuropediatrics. 2018. PMID: 29558773

9

[25 Years of ESPED as a Surveillance Tool for Rare Diseases in Children in Germany: A Critical Analysis].

Ebrahimi-Fakhari D, Zemlin M, Sauer H, Poryo M, Graf N, Meyer S. Ebrahimi-Fakhari D, et al. Klin Padiatr. 2018 Jul;230(4):215-224. doi: 10.1055/a-0586-4365. Epub 2018 Apr 3. Klin Padiatr. 2018. PMID: 29614515 German.

10

Incidence of tuberous sclerosis and age at first diagnosis: new data and emerging trends from a national, prospective surveillance study.

Ebrahimi-Fakhari D, Mann LL, Poryo M, Graf N, von Kries R, Heinrich B, Ebrahimi-Fakhari D, Flotats-Bastardas M, Gortner L, Zemlin M, Meyer S. Ebrahimi-Fakhari D, et al. Orphanet J Rare Dis. 2018 Jul 17;13(1):117. doi: 10.1186/s13023-018-0870-y. Orphanet J Rare Dis. 2018. PMID: 30016967 Free PMC article.

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