نتائج البحث

Infusion parameters, safety, and practical guidance for the manual administration of subcutaneous immunoglobulin 20% (Ig20Gly).

• Authors : Grosse-Kreul, Dorothea¹ (AUTHOR) ; Allen, Crystal^2,3,4 (AUTHOR); Kalicinsky, Chrystyna⁵ (AUTHOR)

• Source: Allergy, Asthma & Clinical Immunology. 10/4/2024, Vol. 20 Issue 1, p1-12. 12p.

تفاصيل العنوان

fSCIG 10% in pediatric primary immunodeficiency diseases: a European post-authorization safety study.

• Authors : Čižnár, Peter¹ (AUTHOR); Roderick, Marion² (AUTHOR); Schneiderova, Helen³ (AUTHOR)

• Source: Allergy, Asthma & Clinical Immunology. 9/17/2024, Vol. 20 Issue 1, p1-9. 9p.

تفاصيل العنوان

Mycoplasma pneumonia in a patient with X-linked agammaglobulinemia.

• Authors : Dai, Bowen^1,2 (AUTHOR); Han, Shujuan¹ (AUTHOR); Shen, Yuanfang¹ (AUTHOR)

• Source: BMC Infectious Diseases. 9/13/2024, Vol. 24 Issue 1, p1-5. 5p.

تفاصيل العنوان

Time to diagnosis for a rare disease: managing medical uncertainty. A qualitative study.

• Authors : Phillips, Christine¹ (AUTHOR); Parkinson, Anne² (AUTHOR) ; Namsrai, Tergel² (AUTHOR)

• Source: Orphanet Journal of Rare Diseases. 8/14/2024, Vol. 19 Issue 1, p1-10. 10p.

تفاصيل العنوان

Pyogenic liver abscess in pediatric populations in beijing (2008–2023).

• Authors : Xie, Yue¹ (AUTHOR); Guo, Ling-yun¹ (AUTHOR); Liu, Bing¹ (AUTHOR)

Subjects: *PYOGENIC liver abscess; *CHILD patients; *LIVER abscessesBEIJING (China); CHINA

• Source: BMC Infectious Diseases. 7/29/2024, Vol. 24 Issue 1, p1-8. 8p.

تفاصيل العنوان

Interstitial lung diseases (ILD) in common variable immunodeficiency (CVID) patients: a study from Iran.

• Authors : Khanbabaee, Ghamartaj¹ (AUTHOR); khazaii, Fatemeh¹ (AUTHOR) ; Chavoshzadeh, Zahra² (AUTHOR)

• Source: BMC Immunology. 7/16/2024, Vol. 25 Issue 1, p1-7. 7p.

تفاصيل العنوان

COVID-19 in patients with thymic epithelial tumors with or without Good's syndrome: a single-center retrospective study.

• Authors : Pietroluongo E; Department of Clinical Medicine and Surgery, University of Naples Federico II, Naples, Italy.; Peddio A

Subjects: COVID-19*/COVID-19*/COVID-19*/complications ; COVID-19*/COVID-19*/COVID-19*/epidemiology ; COVID-19*/COVID-19*/COVID-19*/immunology Thymic epithelial tumor

• Source: BMC cancer [BMC Cancer] 2024 Jun 19; Vol. 24 (1), pp. 748. Date of Electronic Publication: 2024 Jun 19.Publisher: BioMed Central Country of Publication: England NLM ID: 100967800 Publication Model: Electronic Cited Medium:

تفاصيل العنوان

Activated phosphoinositde 3-kinase (PI3Kδ) syndrome: an Italian point of view on diagnosis and new advances in treatment.

• Authors : Lougaris V; Pediatrics Clinic, Department of Clinical and Experimental Sciences, University of Brescia, Azienda Socio Sanitaria Territoriale Spedali Civili di Brescia, Brescia, Italy.; Piane FL

Subjects: Class I Phosphatidylinositol 3-Kinases* ; Primary Immunodeficiency Diseases*/Primary Immunodeficiency Diseases*/Primary Immunodeficiency Diseases*/diagnosis ; Primary Immunodeficiency Diseases*/Primary Immunodeficiency Diseases*/Primary Immunodeficiency Diseases*/therapyActivated PI3K-delta Syndrome

• Source: Italian journal of pediatrics [Ital J Pediatr] 2024 May 20; Vol. 50 (1), pp. 103. Date of Electronic Publication: 2024 May 20.Publisher: BioMed Central Country of Publication: England NLM ID: 101510759 Publication Model: Electronic Cited Medium:

تفاصيل العنوان

Altered oral microbiome, but normal human papilloma virus prevalence in cartilage-hair hypoplasia patients.

• Authors : Arponen H; Department of Oral and Maxillofacial Diseases, Helsinki University Hospital Head and Neck Center, University of Helsinki, Haartmaninkatu 1, Helsinki, Finland. .; Pediatric Research Center, Children's Hospital, University of Helsinki, Helsinki University Hospital, Helsinki, Finland. .

Subjects: Hair*/Hair*/Hair*/abnormalities ; Hirschsprung Disease* ; Microbiota* Cartilage-hair hypoplasia

• Source: Orphanet journal of rare diseases [Orphanet J Rare Dis] 2024 Apr 18; Vol. 19 (1), pp. 169. Date of Electronic Publication: 2024 Apr 18.Publisher: BioMed Central Country of Publication: England NLM ID: 101266602 Publication Model: Electronic Cited Medium:

تفاصيل العنوان

Activated phosphoinositide 3-kinase δ syndrome caused by PIK3CD mutations: expanding the phenotype.

• Authors : Zhao, Peiwei; Huang, Juan; Fu, Huicong

Subjects: PHOSPHATIDYLINOSITOL 3-kinases; PRIMARY immunodeficiency diseases; SYMPTOMS

• Source: Pediatric Rheumatology; 1/29/2024, Vol. 22 Issue 1, p1-8, 8p

تفاصيل العنوان