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

Year Number of Results
1954 1
1955 2
1956 2
1959 1
1974 1
1975 1
1977 2
1978 4
1979 1
1980 2
1981 2
1982 5
1983 1
1984 1
1985 2
1989 1
1990 3
1991 7
1992 2
1993 3
1994 2
1996 5
1997 2
1998 2
1999 5
2000 4
2001 4
2002 4
2003 2
2004 1
2005 3
2006 5
2007 7
2008 7
2009 7
2010 7
2011 13
2012 12
2013 19
2014 20
2015 12
2016 13
2017 16
2018 14
2019 28
2020 21
2021 24
2022 20
2023 27
2024 32
2025 17

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362 results

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Page 1
Overview of secondary immunodeficiency.
Herman KE, Tuttle KL. Herman KE, et al. Allergy Asthma Proc. 2024 Sep 1;45(5):347-354. doi: 10.2500/aap.2024.45.240063. Allergy Asthma Proc. 2024. PMID: 39294908 Review.
Pharmacomechanical Catheter-Directed Thrombolysis for Deep-Vein Thrombosis.
Vedantham S, Goldhaber SZ, Julian JA, Kahn SR, Jaff MR, Cohen DJ, Magnuson E, Razavi MK, Comerota AJ, Gornik HL, Murphy TP, Lewis L, Duncan JR, Nieters P, Derfler MC, Filion M, Gu CS, Kee S, Schneider J, Saad N, Blinder M, Moll S, Sacks D, Lin J, Rundback J, Garcia M, Razdan R, VanderWoude E, Marques V, Kearon C; ATTRACT Trial Investigators. Vedantham S, et al. N Engl J Med. 2017 Dec 7;377(23):2240-2252. doi: 10.1056/NEJMoa1615066. N Engl J Med. 2017. PMID: 29211671 Free PMC article. Clinical Trial.
Disruptive mutations in TANC2 define a neurodevelopmental syndrome associated with psychiatric disorders.
Guo H, Bettella E, Marcogliese PC, Zhao R, Andrews JC, Nowakowski TJ, Gillentine MA, Hoekzema K, Wang T, Wu H, Jangam S, Liu C, Ni H, Willemsen MH, van Bon BW, Rinne T, Stevens SJC, Kleefstra T, Brunner HG, Yntema HG, Long M, Zhao W, Hu Z, Colson C, Richard N, Schwartz CE, Romano C, Castiglia L, Bottitta M, Dhar SU, Erwin DJ, Emrick L, Keren B, Afenjar A, Zhu B, Bai B, Stankiewicz P, Herman K; University of Washington Center for Mendelian Genomics; Mercimek-Andrews S, Juusola J, Wilfert AB, Abou Jamra R, Büttner B, Mefford HC, Muir AM, Scheffer IE, Regan BM, Malone S, Gecz J, Cobben J, Weiss MM, Waisfisz Q, Bijlsma EK, Hoffer MJV, Ruivenkamp CAL, Sartori S, Xia F, Rosenfeld JA, Bernier RA, Wangler MF, Yamamoto S, Xia K, Stegmann APA, Bellen HJ, Murgia A, Eichler EE. Guo H, et al. Among authors: herman k. Nat Commun. 2019 Oct 15;10(1):4679. doi: 10.1038/s41467-019-12435-8. Nat Commun. 2019. PMID: 31616000 Free PMC article.
Tuberculous Epididymitis.
Herman KO, Lee ER. Herman KO, et al. Ultrasound Q. 2015 Sep;31(3):202-4. doi: 10.1097/RUQ.0000000000000135. Ultrasound Q. 2015. PMID: 25945724 No abstract available.
Configural frequency trees.
Wiedermann W, Herman KC, Reinke W, von Eye A. Wiedermann W, et al. Among authors: herman kc. Dev Psychopathol. 2022 Oct;34(4):1585-1603. doi: 10.1017/S0954579421000018. Epub 2021 Mar 10. Dev Psychopathol. 2022. PMID: 33750489
Updates to the role of diet in atopic dermatitis.
Herman KE, Beck LA, Järvinen KM. Herman KE, et al. J Am Acad Dermatol. 2025 Aug;93(2):e55-e56. doi: 10.1016/j.jaad.2025.02.096. Epub 2025 Mar 29. J Am Acad Dermatol. 2025. PMID: 40164384 No abstract available.
Heterozygous de novo variants in HSPD1 cause hypomyelinating leukodystrophy through impaired HSP60 oligomerisation.
Eskin-Schwartz M, Seraidy S, Paz E, Molhem M, Ranza E, Antonarakis SE, Blanc X, Herman K, Benko WS, Libzon S, Ben Sira L, Fattal-Valevski A, Dolgin V, Birk OS, Kessel A, Bross P, Weiss C, Azem A, Zerem A. Eskin-Schwartz M, et al. Among authors: herman k. J Med Genet. 2024 Dec 31;62(1):15-24. doi: 10.1136/jmg-2024-109862. J Med Genet. 2024. PMID: 39500555
362 results