Delayed Adrenarche may be an Additional Feature of Immunoglobulin Super Family Member 1 Deficiency Syndrome.
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Rare Variants in Complement Gene in C3 Glomerulopathy and Immunoglobulin-Mediated Membranoproliferative GN.
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Treatment of FSGS in Children.
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Autoimmunity and Delayed Diagnosis in Pediatric Idiopathic Pulmonary Hemosiderosis.
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J Pediatr Hematol Oncol. 2020 May;42(4):e240-e243. doi: 10.1097/MPH.0000000000001513.
Immunotherapy for primary immunodeficiency diseases.
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Med Clin North Am. 2012 May;96(3):433-54, ix. doi: 10.1016/j.mcna.2012.04.010. Epub 2012 May 22.
IGSF1 deficiency syndrome: A newly uncovered endocrinopathy.
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Rare Dis. 2013 May 2;1:e24883. doi: 10.4161/rdis.24883. eCollection 2013.
Neurological Involvement in Childhood Evans Syndrome.
Pincez T, Neven B, Le Pointe HD, Varlet P, Fernandes H, Gareton A, Leverger G, Leblanc T, Chambost H, Michel G, Pasquet M, Millot F, Hermine O, Mathian A, Hully M, Zephir H, Hamidou M, Durand JM, Perel Y, Landman-Parker J, Rieux-Laucat F, Aladjidi N.
J Clin Immunol. 2019 Feb;39(2):171-181. doi: 10.1007/s10875-019-0594-3. Epub 2019 Jan 22.
Idiopathic late-onset immunoglobulin deficiency with functional T-cell deficiency.
Wilson WR, Hermans PE, Ritts RE Jr.
Arch Intern Med. 1976 Mar;136(3):343-6.
Post-Viral Acquired Idiopathic Purpura Fulminans Caused by Anti-Protein S Antibodies.
Theron A, Biron-Andreani C, Jeziorski E.
Acta Paediatr. 2025 Jun 23. doi: 10.1111/apa.70193. Online ahead of print.
