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Page 1
ATTR amyloidosis during the COVID-19 pandemic: insights from a global medical roundtable.
Brannagan TH 3rd, Auer-Grumbach M, Berk JL, Briani C, Bril V, Coelho T, Damy T, Dispenzieri A, Drachman BM, Fine N, Gaggin HK, Gertz M, Gillmore JD, Gonzalez E, Hanna M, Hurwitz DR, Khella SL, Maurer MS, Nativi-Nicolau J, Olugemo K, Quintana LF, Rosen AM, Schmidt HH, Shehata J, Waddington-Cruz M, Whelan C, Ruberg FL. Brannagan TH 3rd, et al. Among authors: auer grumbach m. Orphanet J Rare Dis. 2021 May 6;16(1):204. doi: 10.1186/s13023-021-01834-0. Orphanet J Rare Dis. 2021. PMID: 33957949 Free PMC article.
Chance or challenge, spoilt for choice? New recommendations on diagnostic and therapeutic considerations in hereditary transthyretin amyloidosis with polyneuropathy: the German/Austrian position and review of the literature.
Dohrn MF, Auer-Grumbach M, Baron R, Birklein F, Escolano-Lozano F, Geber C, Grether N, Hagenacker T, Hund E, Sachau J, Schilling M, Schmidt J, Schulte-Mattler W, Sommer C, Weiler M, Wunderlich G, Hahn K. Dohrn MF, et al. J Neurol. 2021 Oct;268(10):3610-3625. doi: 10.1007/s00415-020-09962-6. Epub 2020 Jun 4. J Neurol. 2021. PMID: 32500375 Free PMC article.
Diagnosis and treatment of cardiac amyloidosis: an interdisciplinary consensus statement.
Bonderman D, Pölzl G, Ablasser K, Agis H, Aschauer S, Auer-Grumbach M, Binder C, Dörler J, Duca F, Ebner C, Hacker M, Kain R, Kammerlander A, Koschutnik M, Kroiss AS, Mayr A, Nitsche C, Rainer PP, Reiter-Malmqvist S, Schneider M, Schwarz R, Verheyen N, Weber T, Zaruba MM, Badr Eslam R, Hülsmann M, Mascherbauer J. Bonderman D, et al. Among authors: auer grumbach m. Wien Klin Wochenschr. 2020 Dec;132(23-24):742-761. doi: 10.1007/s00508-020-01781-z. Epub 2020 Dec 3. Wien Klin Wochenschr. 2020. PMID: 33270160 Free PMC article.
Hereditary sensory neuropathy type I.
Auer-Grumbach M. Auer-Grumbach M. Orphanet J Rare Dis. 2008 Mar 18;3:7. doi: 10.1186/1750-1172-3-7. Orphanet J Rare Dis. 2008. PMID: 18348718 Free PMC article. Review.
Hereditary ATTR Amyloidosis in Austria: Prevalence and Epidemiological Hot Spots.
Auer-Grumbach M, Rettl R, Ablasser K, Agis H, Beetz C, Duca F, Gattermeier M, Glaser F, Hacker M, Kain R, Kaufmann B, Kovacs GG, Lampl C, Ljevakovic N, Nagele J, Pölzl G, Quasthoff S, Raimann B, Rauschka H, Reiter C, Skrahina V, Schuhfried O, Sunder-Plassmann R, Verheyen ND, Wanschitz J, Weber T, Windhager R, Wurm R, Zimprich F, Löscher WN, Bonderman D. Auer-Grumbach M, et al. J Clin Med. 2020 Jul 14;9(7):2234. doi: 10.3390/jcm9072234. J Clin Med. 2020. PMID: 32674397 Free PMC article.
Convolutional Neural Networks for Fully Automated Diagnosis of Cardiac Amyloidosis by Cardiac Magnetic Resonance Imaging.
Agibetov A, Kammerlander A, Duca F, Nitsche C, Koschutnik M, Donà C, Dachs TM, Rettl R, Stria A, Schrutka L, Binder C, Kastner J, Agis H, Kain R, Auer-Grumbach M, Samwald M, Hengstenberg C, Dorffner G, Mascherbauer J, Bonderman D. Agibetov A, et al. Among authors: auer grumbach m. J Pers Med. 2021 Dec 1;11(12):1268. doi: 10.3390/jpm11121268. J Pers Med. 2021. PMID: 34945740 Free PMC article.
Hereditary sensory neuropathies.
Auer-Grumbach M. Auer-Grumbach M. Drugs Today (Barc). 2004 May;40(5):385-94. doi: 10.1358/dot.2004.40.5.850487. Drugs Today (Barc). 2004. PMID: 15319794 Review.
Targeted high-throughput sequencing identifies mutations in atlastin-1 as a cause of hereditary sensory neuropathy type I.
Guelly C, Zhu PP, Leonardis L, Papić L, Zidar J, Schabhüttl M, Strohmaier H, Weis J, Strom TM, Baets J, Willems J, De Jonghe P, Reilly MM, Fröhlich E, Hatz M, Trajanoski S, Pieber TR, Janecke AR, Blackstone C, Auer-Grumbach M. Guelly C, et al. Am J Hum Genet. 2011 Jan 7;88(1):99-105. doi: 10.1016/j.ajhg.2010.12.003. Epub 2010 Dec 30. Am J Hum Genet. 2011. PMID: 21194679 Free PMC article.
112 results