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

Year Number of Results
1966 1
1967 1
1969 1
1970 2
1971 1
1972 2
1974 1
1975 8
1976 5
1977 10
1978 7
1979 7
1980 3
1981 6
1982 4
1983 3
1984 12
1985 10
1986 8
1987 5
1988 15
1989 14
1990 18
1991 18
1992 15
1993 23
1994 19
1995 21
1996 13
1997 16
1998 18
1999 8
2000 19
2001 6
2002 8
2003 15
2004 9
2005 10
2006 7
2007 7
2008 7
2009 9
2010 6
2011 6
2012 10
2013 2
2014 7
2015 4
2016 5
2018 1
2019 3
2020 3
2021 1
2022 1
2024 0

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431 results

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Page 1
Initial presenting manifestations in 16,486 patients with inborn errors of immunity include infections and noninfectious manifestations.
Thalhammer J, Kindle G, Nieters A, Rusch S, Seppänen MRJ, Fischer A, Grimbacher B, Edgar D, Buckland M, Mahlaoui N, Ehl S; European Society for Immunodeficiencies Registry Working Party. Thalhammer J, et al. J Allergy Clin Immunol. 2021 Nov;148(5):1332-1341.e5. doi: 10.1016/j.jaci.2021.04.015. Epub 2021 Apr 23. J Allergy Clin Immunol. 2021. PMID: 33895260 Free article.
Autologous hematopoietic stem cell transplantation vs intravenous pulse cyclophosphamide in diffuse cutaneous systemic sclerosis: a randomized clinical trial.
van Laar JM, Farge D, Sont JK, Naraghi K, Marjanovic Z, Larghero J, Schuerwegh AJ, Marijt EW, Vonk MC, Schattenberg AV, Matucci-Cerinic M, Voskuyl AE, van de Loosdrecht AA, Daikeler T, Kötter I, Schmalzing M, Martin T, Lioure B, Weiner SM, Kreuter A, Deligny C, Durand JM, Emery P, Machold KP, Sarrot-Reynauld F, Warnatz K, Adoue DF, Constans J, Tony HP, Del Papa N, Fassas A, Himsel A, Launay D, Lo Monaco A, Philippe P, Quéré I, Rich É, Westhovens R, Griffiths B, Saccardi R, van den Hoogen FH, Fibbe WE, Socié G, Gratwohl A, Tyndall A; EBMT/EULAR Scleroderma Study Group. van Laar JM, et al. JAMA. 2014 Jun 25;311(24):2490-8. doi: 10.1001/jama.2014.6368. JAMA. 2014. PMID: 25058083 Free article. Clinical Trial.
Relevance of biallelic versus monoallelic TNFRSF13B mutations in distinguishing disease-causing from risk-increasing TNFRSF13B variants in antibody deficiency syndromes.
Salzer U, Bacchelli C, Buckridge S, Pan-Hammarström Q, Jennings S, Lougaris V, Bergbreiter A, Hagena T, Birmelin J, Plebani A, Webster AD, Peter HH, Suez D, Chapel H, McLean-Tooke A, Spickett GP, Anover-Sombke S, Ochs HD, Urschel S, Belohradsky BH, Ugrinovic S, Kumararatne DS, Lawrence TC, Holm AM, Franco JL, Schulze I, Schneider P, Gertz EM, Schäffer AA, Hammarström L, Thrasher AJ, Gaspar HB, Grimbacher B. Salzer U, et al. Among authors: peter hh. Blood. 2009 Feb 26;113(9):1967-76. doi: 10.1182/blood-2008-02-141937. Epub 2008 Nov 3. Blood. 2009. PMID: 18981294 Free PMC article.
The genetics of hypogammaglobulinemia.
Grimbacher B, Schäffer AA, Peter HH. Grimbacher B, et al. Among authors: peter hh. Curr Allergy Asthma Rep. 2004 Sep;4(5):349-58. doi: 10.1007/s11882-004-0083-4. Curr Allergy Asthma Rep. 2004. PMID: 15283873 Review.
[Chronic periaortitis].
Pipitone N, Salvarani C, Peter HH. Pipitone N, et al. Among authors: peter hh. Internist (Berl). 2010 Jan;51(1):45-52. doi: 10.1007/s00108-009-2407-x. Internist (Berl). 2010. PMID: 19997897 German.
Common variable immunodeficiency: an update.
Salzer U, Warnatz K, Peter HH. Salzer U, et al. Among authors: peter hh. Arthritis Res Ther. 2012 Sep 24;14(5):223. doi: 10.1186/ar4032. Arthritis Res Ther. 2012. PMID: 23043756 Free PMC article. Review.
[Paroxysmal nocturnal hemoglobinuria].
Blaas P, Weber S, Hänsch GM, Peter HH. Blaas P, et al. Among authors: peter hh. Klin Wochenschr. 1990 Mar 5;68(5):247-55. doi: 10.1007/BF02116052. Klin Wochenschr. 1990. PMID: 2182938 Review. German.
431 results