Ramsay Fuleihan
Overview
Explore the profile of Ramsay Fuleihan including associated specialties, affiliations and a list of published articles.
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Articles
30
Citations
656
Followers
0
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Recent Articles
1.
Materne E, Zhou B, DiGiacomo D, Farmer J, Fuleihan R, Sullivan K, et al.
J Allergy Clin Immunol
. 2024 Mar;
154(1):237-242.e1.
PMID: 38555979
Background: Prior studies have reported that renal insufficiency occurs in a small percentage of patients with predominantly antibody deficiency (PAD) and in about 2% of patients with common variable immunodeficiency....
2.
Gunderman L, Brown J, Chaudhury S, OGorman M, Fuleihan R, Khanolkar A, et al.
Biomedicines
. 2023 Mar;
11(3).
PMID: 36979938
We present a unique and unusual case of a male patient diagnosed with two coexisting and typically unassociated X-linked conditions: he was initially diagnosed with X-linked agammaglobulinemia (XLA) followed by...
3.
Krase I, Garabedian E, Fuleihan R, Sacco K
Clin Immunol
. 2022 Oct;
245:109135.
PMID: 36184050
No abstract available.
4.
El-Sayed Z, El-Ghoneimy D, Ortega-Martell J, Radwan N, Aldave J, Al-Herz W, et al.
World Allergy Organ J
. 2022 Jul;
15(6):100657.
PMID: 35783543
Background: Allergies have long been observed in Inborn Errors of Immunity (IEI) and might even be the first presentation resulting in delayed diagnosis or misdiagnosis in some cases. However, data...
5.
Demirdag Y, Fuleihan R, Orange J, Yu J
Curr Opin Pediatr
. 2021 Oct;
33(6):657-675.
PMID: 34670265
Purpose Of Review: Primary immunodeficiency diseases (PIDs), also called inborn errors of immunity (IEI), are genetic disorders classically characterized by an increased susceptibility to infection and/or disruption in the regulation...
6.
Oh J, Garabedian E, Fuleihan R, Cunningham-Rundles C
J Allergy Clin Immunol Pract
. 2021 Aug;
9(11):4095-4102.
PMID: 34352450
Background: Activated phosphoinositide 3-kinase δ syndrome is a combined primary immunodeficiency characterized by gain-of-function mutations in PIK3CD and PIK3R1. Activated phosphoinositide 3-kinase δ syndrome demonstrates a large range of phenotypes...
7.
Le Voyer T, Sakata S, Tsumura M, Khan T, Esteve-Sole A, Al-Saud B, et al.
J Immunol
. 2021 Jun;
207(1):133-152.
PMID: 34183371
Autosomal recessive (AR) STAT1 deficiency is a severe inborn error of immunity disrupting cellular responses to type I, II, and III IFNs, and IL-27, and conferring a predisposition to both...
8.
Lee M, Nguyen J, Fuleihan R, Gundling K, Cunningham-Rundles C, Otani I
J Clin Immunol
. 2020 Sep;
40(8):1181-1183.
PMID: 32901355
No abstract available.
9.
Kellner E, Fuleihan R, Cunningham-Rundles C, Wechsler J
J Clin Immunol
. 2019 Jun;
39(6):569-576.
PMID: 31250334
Purpose: Chronic lung disease is the most common cause of morbidity and mortality in patients with common variable immunodeficiency (CVID). While biomarkers exist to predict non-infectious complications, the unique features...
10.
Weinberger T, Fuleihan R, Cunningham-Rundles C, Maglione P
J Clin Immunol
. 2019 May;
39(4):440-447.
PMID: 31089938
Purpose: Pulmonary complications occur frequently in primary antibody deficiency (PAD). While the impact of antibody deficiency may appear implicit for certain respiratory infections, immunoglobulin replacement therapy does not completely ameliorate...