Schmitt-Graeff A - Search Results

1

17q12 Deletion Syndrome as a Rare Cause for Diabetes Mellitus Type MODY5.

Roehlen N, Hilger H, Stock F, Gläser B, Guhl J, Schmitt-Graeff A, Seufert J, Laubner K. Roehlen N, et al. J Clin Endocrinol Metab. 2018 Oct 1;103(10):3601-3610. doi: 10.1210/jc.2018-00955. J Clin Endocrinol Metab. 2018. PMID: 30032214 Review.

2

[Granulocytic sarcoma (so-called chloroma) as a possible cause of spinal cord compression. Case report and differential diagnosis].

Niedermayer I, Schmitt-Graeff A, Kölbel CB, Hertel F, Feiden W. Niedermayer I, et al. Pathologe. 2000 Jan;21(1):82-5. doi: 10.1007/s002920050009. Pathologe. 2000. PMID: 10663672 German.

3

Fatal hemophagocytic syndrome in a patient with a previously well-controlled asymptomatic HIV infection after EBV reactivation.

Thoden J, Rieg S, Venhoff N, Wennekes V, Schmitt-Graeff A, Wagner D, Kern WV. Thoden J, et al. J Infect. 2012 Jan;64(1):110-2. doi: 10.1016/j.jinf.2011.08.011. Epub 2011 Aug 23. J Infect. 2012. PMID: 21888928

4

[Primary cutaneous lymphoma-a case series of 163 patients].

Nashan D, Friedrich CM, Geissler E, Schmitt-Graeff A, Klein F, Meiss F. Nashan D, et al. Hautarzt. 2018 Dec;69(12):1014-1020. doi: 10.1007/s00105-018-4212-8. Hautarzt. 2018. PMID: 29881891 German.

5

Diagnostic and therapeutic challenge of unclassifiable enteropathies with increased intraepithelial CD103⁺ CD8⁺ T lymphocytes: a single center case series.

Hartl C, Finke J, Hasselblatt P, Kreisel W, Schmitt-Graeff A. Hartl C, et al. Scand J Gastroenterol. 2021 Aug;56(8):889-898. doi: 10.1080/00365521.2021.1931958. Epub 2021 May 31. Scand J Gastroenterol. 2021. PMID: 34057863

6

Chronic inflammatory bowel disease as key manifestation of atypical ARTEMIS deficiency.

Rohr J, Pannicke U, Döring M, Schmitt-Graeff A, Wiech E, Busch A, Speckmann C, Müller I, Lang P, Handgretinger R, Fisch P, Schwarz K, Ehl S. Rohr J, et al. J Clin Immunol. 2010 Mar;30(2):314-20. doi: 10.1007/s10875-009-9349-x. Epub 2009 Dec 5. J Clin Immunol. 2010. PMID: 19967552

7

IgG4-related disease in autoimmune lymphoproliferative syndrome.

van de Ven AAJM, Seidl M, Drendel V, Schmitt-Graeff A, Voll RE, Rensing-Ehl A, Speckmann C, Ehl S, Warnatz K, Kollert F. van de Ven AAJM, et al. Clin Immunol. 2017 Jul;180:97-99. doi: 10.1016/j.clim.2017.05.003. Epub 2017 May 3. Clin Immunol. 2017. PMID: 28478106

8

Loss of the Fanconi anemia-associated protein NIPA causes bone marrow failure.

Kreutmair S, Erlacher M, Andrieux G, Istvanffy R, Mueller-Rudorf A, Zwick M, Rückert T, Pantic M, Poggio T, Shoumariyeh K, Mueller TA, Kawaguchi H, Follo M, Klingeberg C, Wlodarski M, Baumann I, Pfeifer D, Kulinski M, Rudelius M, Lemeer S, Kuster B, Dierks C, Peschel C, Cabezas-Wallscheid N, Duque-Afonso J, Zeiser R, Cleary ML, Schindler D, Schmitt-Graeff A, Boerries M, Niemeyer CM, Oostendorp RA, Duyster J, Illert AL. Kreutmair S, et al. J Clin Invest. 2020 Jun 1;130(6):2827-2844. doi: 10.1172/JCI126215. J Clin Invest. 2020. PMID: 32338640 Free PMC article.

9

Ill-defined germinal centers and severely reduced plasma cells are histological hallmarks of lymphadenopathy in patients with common variable immunodeficiency.

Unger S, Seidl M, Schmitt-Graeff A, Böhm J, Schrenk K, Wehr C, Goldacker S, Dräger R, Gärtner BC, Fisch P, Werner M, Warnatz K. Unger S, et al. J Clin Immunol. 2014 Aug;34(6):615-26. doi: 10.1007/s10875-014-0052-1. Epub 2014 May 2. J Clin Immunol. 2014. PMID: 24789743

10

Esophageal lichen planus: towards diagnosis of an underdiagnosed disease.

Schauer F, Monasterio C, Technau-Hafsi K, Kern JS, Lazaro A, Deibert P, Hasselblatt P, Schwacha H, Heeg S, Brass V, Küllmer A, Schmidt AR, Schmitt-Graeff A, Kreisel W. Schauer F, et al. Scand J Gastroenterol. 2019 Oct;54(10):1189-1198. doi: 10.1080/00365521.2019.1674375. Epub 2019 Oct 14. Scand J Gastroenterol. 2019. PMID: 31608788

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