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Quoted phrase not found in phrase index: "Immunoglobulin heavy chain deficiency"
Page 1
Immunoglobulin A nephropathy: a pathophysiology view.
Fabiano RC, Pinheiro SV, Simões E Silva AC. Fabiano RC, et al. Inflamm Res. 2016 Oct;65(10):757-70. doi: 10.1007/s00011-016-0962-x. Epub 2016 Jun 28. Inflamm Res. 2016. PMID: 27351940 Review.
RESULTS: Current studies indicate an ordered sequence of multi-hits as fundamental to disease occurrence. Altered glycan structures in the hinge region of the heavy chains of IgA1 molecules act as auto-antigens, potentially triggering the production of glycan-specif …
RESULTS: Current studies indicate an ordered sequence of multi-hits as fundamental to disease occurrence. Altered glycan structures in the h …
Heavy Chain Deposition Disease: Clinicopathologic Characteristics of a Chinese Case Series.
Zhang Y, Li X, Liang D, Xu F, Liang S, Zhu X, Zheng N, Huang X, Liu Z, Zeng C. Zhang Y, et al. Am J Kidney Dis. 2020 May;75(5):736-743. doi: 10.1053/j.ajkd.2019.08.013. Epub 2019 Nov 5. Am J Kidney Dis. 2020. PMID: 31699519
RATIONALE & OBJECTIVE: Heavy chain deposition disease (HCDD) is a rare consequence of monoclonal immunoglobulin deposition disease that has not been well characterized in non-white populations. ...CONCLUSIONS: In this case series of HCDD in a single cente …
RATIONALE & OBJECTIVE: Heavy chain deposition disease (HCDD) is a rare consequence of monoclonal immunoglobulin dep …
Clinical criteria for the diagnosis of vascular dementia.
Loeb C. Loeb C. Eur Neurol. 1988;28(2):87-92. doi: 10.1159/000116237. Eur Neurol. 1988. PMID: 3131146 Review.
The usual ancillary diagnostic investigations (biochemical tests, cerebrospinal fluid (CSF), EEG, CT, MRI, angiography) can rather easily identify brain disorders due to tumors, vascular malformations, hematomas, infections, toxins and drugs, deficiency diseases, normal-pr …
The usual ancillary diagnostic investigations (biochemical tests, cerebrospinal fluid (CSF), EEG, CT, MRI, angiography) can rather easily id …
Immunoglobulin deficiency syndromes and therapy.
Huston DP, Kavanaugh AF, Rohane PW, Huston MM. Huston DP, et al. J Allergy Clin Immunol. 1991 Jan;87(1 Pt 1):1-17. doi: 10.1016/0091-6749(91)90203-z. J Allergy Clin Immunol. 1991. PMID: 1704022 Review. No abstract available.
Two pediatric oncologic cases of hypereosinophilic syndrome and review of the literature.
Voeller J, DeNapoli T, Griffin TC. Voeller J, et al. Cancer Rep (Hoboken). 2022 Nov;5(11):e1710. doi: 10.1002/cnr2.1710. Epub 2022 Oct 14. Cancer Rep (Hoboken). 2022. PMID: 36241191 Free PMC article. Review.
He was ultimately diagnosed with precursor B-cell acute lymphoblastic leukemia with immunoglobulin heavy chain gene rearrangement. He completed standard treatment without significant complications and remains in remission at about 2 years off therapy. He is i …
He was ultimately diagnosed with precursor B-cell acute lymphoblastic leukemia with immunoglobulin heavy chain gene rea …
Camelid single-domain antibody fragments: Uses and prospects to investigate protein misfolding and aggregation, and to treat diseases associated with these phenomena.
Pain C, Dumont J, Dumoulin M. Pain C, et al. Biochimie. 2015 Apr;111:82-106. doi: 10.1016/j.biochi.2015.01.012. Epub 2015 Feb 3. Biochimie. 2015. PMID: 25656912 Free article. Review.
In this review, we focus on how VHHs or nanobodies, the antigen-binding domains of camelid heavy-chain antibodies, are being increasingly used to characterise each of the species formed on the pathway of fibril formation in terms of structure, stability, kinetics of …
In this review, we focus on how VHHs or nanobodies, the antigen-binding domains of camelid heavy-chain antibodies, are being i …
IgG subclass deficiency with or without IgA deficiency.
Hanson LA, Söderström R, Nilssen DE, Theman K, Björkander J, Söderström T, Karlsson G, Brandtzaeg P. Hanson LA, et al. Clin Immunol Immunopathol. 1991 Nov;61(2 Pt 2):S70-7. doi: 10.1016/s0090-1229(05)80040-6. Clin Immunol Immunopathol. 1991. PMID: 1934615 Review.
IgG subclass deficiency (IgGSD) is difficult to define since reference materials vary between laboratories and the clinically relevant cut off levels for the various subclasses are not well known. ...Still many individuals with this combined deficiency have been rep …
IgG subclass deficiency (IgGSD) is difficult to define since reference materials vary between laboratories and the clinically relevan …
Defects in memory B-cell and plasma cell subsets expressing different immunoglobulin-subclasses in patients with CVID and immunoglobulin subclass deficiencies.
Blanco E, Pérez-Andrés M, Arriba-Méndez S, Serrano C, Criado I, Del Pino-Molina L, Silva S, Madruga I, Bakardjieva M, Martins C, Serra-Caetano A, Romero A, Contreras-Sanfeliciano T, Bonroy C, Sala F, Martín A, Bastida JM, Lorente F, Prieto C, Dávila I, Marcos M, Kalina T, Vlkova M, Chovancova Z, Cordeiro AI, Philippé J, Haerynck F, López-Granados E, Sousa AE, van der Burg M, van Dongen JJM, Orfao A; EuroFlow PID group. Blanco E, et al. J Allergy Clin Immunol. 2019 Sep;144(3):809-824. doi: 10.1016/j.jaci.2019.02.017. Epub 2019 Feb 28. J Allergy Clin Immunol. 2019. PMID: 30826363 Free article.
BACKGROUND: Predominantly antibody deficiencies (PADs) are the most prevalent primary immunodeficiencies, but their B-cell defects and underlying genetic alterations remain largely unknown. OBJECTIVE: We investigated patients with PADs for the distribution of 41 blood B-ce …
BACKGROUND: Predominantly antibody deficiencies (PADs) are the most prevalent primary immunodeficiencies, but their B-cell defects an …
Hypovitaminosis D Is Prevalent in Patients With Renal AL Amyloidosis and Associated With Renal Outcome.
Muchtar E, Drake MT, Leung N, Dispenzieri A, Lacy MQ, Buadi FK, Dingli D, Hayman SR, Kapoor P, Hwa YL, Fonder A, Hobbs M, Gonsalves W, Kourelis TV, Warsame R, Russell S, Go RS, Binder M, Kyle RA, Rajkumar SV, Kumar SK, Gertz MA. Muchtar E, et al. Front Endocrinol (Lausanne). 2022 Jun 21;13:891712. doi: 10.3389/fendo.2022.891712. eCollection 2022. Front Endocrinol (Lausanne). 2022. PMID: 35800433 Free PMC article.
INTRODUCTION: Vitamin D deficiency is common, but no data have been reported on vitamin D levels in light chain (AL) amyloidosis. ...CONCLUSIONS: Hypovitaminosis D is common in AL amyloidosis, particularly among patients with heavy proteinuria. Severe 25(OH)D …
INTRODUCTION: Vitamin D deficiency is common, but no data have been reported on vitamin D levels in light chain (AL) amyloidos …
75 results