Item request has been placed! ×
Item request cannot be made. ×
loading  Processing Request

نتائج البحث

Display Settings
النتائج لكل صفحة: 10
Sort By: Relevance
Filter
  • 1-3 ل  3 نتائج ل ""Lymphohistiocytosis, Hemophagocytic""

فلترة النتائج

Geographic : iran
إعادة تعيين خيارات الفبترة
Item request has been placed! ×
Item request cannot be made. ×
loading  Processing Request
Academic Journal

Comparison of the clinical features and outcome of children with hemophagocytic lymphohistiocytosis (HLH) secondary to visceral leishmaniasis and primary HLH: a single-center study.

Subjects: Leishmaniasis, Visceral/Leishmaniasis, Visceral/Leishmaniasis, Visceral/*complications ; Lymphohistiocytosis, Hemophagocytic/Lymphohistiocytosis, Hemophagocytic/Lymphohistiocytosis, Hemophagocytic/*diagnosis ; Lymphohistiocytosis, Hemophagocytic/Lymphohistiocytosis, Hemophagocytic/Lymphohistiocytosis, Hemophagocytic/*parasitology

  • Source: BMC infectious diseases [BMC Infect Dis] 2021 Aug 02; Vol. 21 (1), pp. 732. Date of Electronic Publication: 2021 Aug 02.Publisher: BioMed Central Country of Publication: England NLM ID: 100968551 Publication Model: Electronic Cited Medium: Internet ISSN: 1471-2334

تفاصيل العنوان

اقرأ على الانترنت اقرأ أكثر حفظ في قائمتي
×
Academic Journal

Molecular findings and clinical manifestations of 18 Iranian children with Griscelli syndrome type 2: Two novel homozygote mutations in RAB27A gene in a patient.

  • Authors : Tajik S; Immunology, Asthma and Allergy Research Institute, Tehran University of Medical Sciences, Tehran, Iran.; Children's Medical Center, Pediatrics Center of Excellence, Tehran University of Medical Sciences, Tehran, Iran.

Subjects: rab GTP-Binding Proteins*/rab GTP-Binding Proteins*/rab GTP-Binding Proteins*/genetics ; rab GTP-Binding Proteins*/rab GTP-Binding Proteins*/rab GTP-Binding Proteins*/metabolism; Primary Immunodeficiency Diseases Griscelli syndrome type 2

  • Source: Scandinavian journal of immunology [Scand J Immunol] 2023 May; Vol. 97 (5), pp. e13264. Date of Electronic Publication: 2023 Mar 21.Publisher: Blackwell Scientific Publications Country of Publication: England NLM ID: 0323767 Publication Model: Print-Electronic Cited Medium: Internet

تفاصيل العنوان

اقرأ على الانترنت اقرأ أكثر حفظ في قائمتي
×
Academic Journal

Clinical and Genetic Analysis of Nine Suspected Familial Haemophagocytic Lymphohistiocytosis Patients for MUNC13-4 Deficiency and Introducing Four Novel Mutations in UNC13D.

  • Authors : Vahidi M; Department of Molecular Genetics, Islamic Azad University, Tabriz, Iran. .; Badalzadeh M

Subjects: Lymphohistiocytosis, Hemophagocytic/Lymphohistiocytosis, Hemophagocytic/Lymphohistiocytosis, Hemophagocytic/*genetics ; Membrane Proteins/Membrane Proteins/Membrane Proteins/*deficiency ; Membrane Proteins/Membrane Proteins/Membrane Proteins/*genetics

  • Source: Iranian journal of allergy, asthma, and immunology [Iran J Allergy Asthma Immunol] 2019 Oct 23; Vol. 18 (5), pp. 487-492. Date of Electronic Publication:Publisher: Tehran University of Medical Sciences Country of Publication: Iran NLM ID: 101146178 Publication Model: Electronic

تفاصيل العنوان

اقرأ على الانترنت اقرأ أكثر حفظ في قائمتي
×
  • 1-3 ل  3 نتائج ل ""Lymphohistiocytosis, Hemophagocytic""