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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1928 1
1932 1
1946 1
1948 1
1951 1
1952 1
1953 1
1954 1
1956 1
1957 5
1958 1
1959 2
1960 1
1961 5
1962 1
1963 6
1964 2
1965 6
1966 1
1967 8
1968 11
1969 11
1970 6
1971 3
1972 5
1973 5
1974 3
1975 3
1976 6
1977 5
1978 10
1979 11
1980 14
1981 17
1982 13
1983 11
1984 15
1985 11
1986 9
1987 13
1988 17
1989 19
1990 14
1991 15
1992 28
1993 29
1994 23
1995 20
1996 17
1997 21
1998 23
1999 38
2000 32
2001 33
2002 29
2003 21
2004 45
2005 29
2006 42
2007 42
2008 46
2009 52
2010 61
2011 67
2012 75
2013 99
2014 100
2015 99
2016 104
2017 115
2018 150
2019 131
2020 158
2021 163
2022 141
2023 132
2024 131
2025 142
2026 64

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2,554 results

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Page 1
Patisiran, an RNAi Therapeutic, for Hereditary Transthyretin Amyloidosis.
Adams D, Gonzalez-Duarte A, O'Riordan WD, Yang CC, Ueda M, Kristen AV, Tournev I, Schmidt HH, Coelho T, Berk JL, Lin KP, Vita G, Attarian S, Planté-Bordeneuve V, Mezei MM, Campistol JM, Buades J, Brannagan TH 3rd, Kim BJ, Oh J, Parman Y, Sekijima Y, Hawkins PN, Solomon SD, Polydefkis M, Dyck PJ, Gandhi PJ, Goyal S, Chen J, Strahs AL, Nochur SV, Sweetser MT, Garg PP, Vaishnaw AK, Gollob JA, Suhr OB. Adams D, et al. Among authors: schmidt hh. N Engl J Med. 2018 Jul 5;379(1):11-21. doi: 10.1056/NEJMoa1716153. N Engl J Med. 2018. PMID: 29972753 Free article. Clinical Trial.
Inotersen Treatment for Patients with Hereditary Transthyretin Amyloidosis.
Benson MD, Waddington-Cruz M, Berk JL, Polydefkis M, Dyck PJ, Wang AK, Planté-Bordeneuve V, Barroso FA, Merlini G, Obici L, Scheinberg M, Brannagan TH 3rd, Litchy WJ, Whelan C, Drachman BM, Adams D, Heitner SB, Conceição I, Schmidt HH, Vita G, Campistol JM, Gamez J, Gorevic PD, Gane E, Shah AM, Solomon SD, Monia BP, Hughes SG, Kwoh TJ, McEvoy BW, Jung SW, Baker BF, Ackermann EJ, Gertz MA, Coelho T. Benson MD, et al. Among authors: schmidt hh. N Engl J Med. 2018 Jul 5;379(1):22-31. doi: 10.1056/NEJMoa1716793. N Engl J Med. 2018. PMID: 29972757 Free PMC article. Clinical Trial.
S2k-Leitlinie Lebertransplantation der Deutschen Gesellschaft für Gastroenterologie, Verdauungs- und Stoffwechselkrankheiten (DGVS) und der Deutschen Gesellschaft für Allgemein- und Viszeralchirurgie (DGAV).
Berg T, Aehling NF, Bruns T, Welker MW, Weismüller T, Trebicka J, Tacke F, Strnad P, Sterneck M, Settmacher U, Seehofer D, Schott E, Schnitzbauer AA, Schmidt HH, Schlitt HJ, Pratschke J, Pascher A, Neumann U, Manekeller S, Lammert F, Klein I, Kirchner G, Guba M, Glanemann M, Engelmann C, Canbay AE, Braun F, Berg CP, Bechstein WO, Becker T, Trautwein C; Collaborators:. Berg T, et al. Among authors: schmidt hh. Z Gastroenterol. 2024 Sep;62(9):1397-1573. doi: 10.1055/a-2255-7246. Epub 2024 Sep 9. Z Gastroenterol. 2024. PMID: 39250961 Free article. German. No abstract available.
Tafamidis for transthyretin familial amyloid polyneuropathy: a randomized, controlled trial.
Coelho T, Maia LF, Martins da Silva A, Waddington Cruz M, Planté-Bordeneuve V, Lozeron P, Suhr OB, Campistol JM, Conceição IM, Schmidt HH, Trigo P, Kelly JW, Labaudinière R, Chan J, Packman J, Wilson A, Grogan DR. Coelho T, et al. Among authors: schmidt hh. Neurology. 2012 Aug 21;79(8):785-92. doi: 10.1212/WNL.0b013e3182661eb1. Epub 2012 Jul 25. Neurology. 2012. PMID: 22843282 Free PMC article. Clinical Trial.
Artificial Intelligence and Network Medicine: Path to Precision Medicine.
Altucci L, Badimon L, Balligand JL, Baumbach J, Catapano AL, Cheng F, DeMeo D, Gupta R, Hacker M, Liu YY, Loscalzo J, Maniscalco S, Menche J, Menichetti G, Parini P, Schmidt HHHW, Zitnik M. Altucci L, et al. Among authors: schmidt hhhw. NEJM AI. 2025 Sep;2(9):10.1056/aira2401229. doi: 10.1056/aira2401229. Epub 2025 Aug 28. NEJM AI. 2025. PMID: 40918693 Free PMC article.
Ca2+/calmodulin-regulated nitric oxide synthases.
Schmidt HH, Pollock JS, Nakane M, Förstermann U, Murad F. Schmidt HH, et al. Cell Calcium. 1992 Jun-Jul;13(6-7):427-34. doi: 10.1016/0143-4160(92)90055-w. Cell Calcium. 1992. PMID: 1380405 Review.
Long-term safety and efficacy of patisiran for hereditary transthyretin-mediated amyloidosis with polyneuropathy: 12-month results of an open-label extension study.
Adams D, Polydefkis M, González-Duarte A, Wixner J, Kristen AV, Schmidt HH, Berk JL, Losada López IA, Dispenzieri A, Quan D, Conceição IM, Slama MS, Gillmore JD, Kyriakides T, Ajroud-Driss S, Waddington-Cruz M, Mezei MM, Planté-Bordeneuve V, Attarian S, Mauricio E, Brannagan TH 3rd, Ueda M, Aldinc E, Wang JJ, White MT, Vest J, Berber E, Sweetser MT, Coelho T; patisiran Global OLE study group. Adams D, et al. Among authors: schmidt hh. Lancet Neurol. 2021 Jan;20(1):49-59. doi: 10.1016/S1474-4422(20)30368-9. Epub 2020 Nov 16. Lancet Neurol. 2021. PMID: 33212063 Free article. Clinical Trial.
2,554 results