Cover Image

Aortoarteritis and cardiomyopathy in a child with Blau Syndrome

Saved in:

Bibliographic Details
Main Authors:	Touitou I (Author), Hasija RP (Author), Khubchandani RP (Author), Khemani C (Author)
Format:	Book
Published:	BMC, 2011-09-01T00:00:00Z.
Subjects:	article
Online Access:	Connect to this object online.
Tags:	Add Tag No Tags, Be the first to tag this record!

Similar Items

Experience with pediatric sarcoidosis at a centre in Mumbai, India
by: Touitou I, et al.
Published: (2011)

Methotrexate in management of dermatomyositis in a child with insulin-dependant diabetes with chronic hepatitis
by: Khubchandan RP, et al.
Published: (2008)

The Guadalajara-Camptodactyly Syndrome-an unusual case
by: Hasija RP, et al.
Published: (2011)

Sleep disorders in patients with juvenile idiopathic arthritis as assessed by the sleep disturbance scale for children
by: Pistorio A, et al.
Published: (2011)

Aortoarteritis with systemic lupus erythematosus and secondary antiphopholipid syndrome
by: Nandini Chakrabarti, et al.
Published: (2012)

Brucellosis - forgotten but not gone
by: Khubchandani RP, et al.
Published: (2008)

Identification of Blau Syndrome disease signatures
by: Valencia X, et al.
Published: (2011)

Blau syndrome: a case report from Palestine
by: Salam Iriqat, et al.
Published: (2021)

Non-specific aortoarteritis (NSAA) in children: a prospective observational study
by: Sanjeev Kumar, et al.
Published: (2021)

Nonspecific aortoarteritis with lesion of the left branch of the pulmonary artery (Takayasu's disease)
by: Saule Abseitova, et al.
Published: (2018)

Ex vivo and in vitro production of pro-inflammatory cytokines in Blau syndrome
by: P. Galozzi, et al.
Published: (2015)

Blau syndrome: A case report of a rare granulomatous disorder
by: Preema Sinha, et al.
Published: (2020)

Nonspecific aortoarteritis as a Cause of Aortic Dissection in a Middle Aged Man
by: O. V. Tsygankova, et al.
Published: (2022)

A familial case of Blau syndrome caused by a novel genetic mutation
by: Woojoong Kim, et al.
Published: (2016)

A Chinese girl of Blau syndrome with renal arteritis and a literature review
by: Qiaoqian Zeng, et al.
Published: (2023)

Tofacitinib effectiveness in Blau syndrome: a case series of Chinese paediatric patients
by: Song Zhang, et al.
Published: (2021)

Blau syndrome with a rare mutation in exon 9 of NOD2 gene
by: Jelena Velickovic, et al.
Published: (2019)

Blau syndrome with hypertension and hepatic granulomas: a case report and literature review
by: Fangling Yao, et al.
Published: (2023)

Clinical phenotype and CARD15 gene mutation with Blau Syndrome in Chinese children and their parents
by: Li C, et al.
Published: (2008)

Incomplete penetrance of NOD2 C483W mutation underlining Blau syndrome
by: Shao-Yu Chang, et al.
Published: (2022)

Emperipolesis and cell death in NOD2-related Blau Syndrome and Crohn's disease
by: Martin Tammy M, et al.
Published: (2011)

Disease patterns in juvenile dermatomyositis patients from Mumbai, India
by: Mankad D, et al.
Published: (2011)

A novel mutation in early‐onset sarcoidosis/Blau syndrome: an association with Propionibacterium acnes
by: Fumiko Okazaki, et al.
Published: (2021)

Joyce Blau l'éternelle chez les Kurdes
by: Clémence Scalbert-Yücel
Published: (2018)

<i>NOD</i>2 Mutation-Associated Case with Blau Syndrome Triggered by BCG Vaccination
by: Akiko Arakawa, et al.
Published: (2021)

Blau syndrome associated with nucleotide-binding oligomerization domain containing 2 mutation in a baby from Malaysia
by: Kin Fon Leong, et al.
Published: (2019)

Monogenic Autoinflammatory Disease Due to Blau Syndrome with Nucleotide Oligomerization Domain 2 Gene Mutation in an Indian Family
by: Suvarna Magar, et al.
Published: (2024)

Whole-exome sequencing in three children with sporadic Blau syndrome, one of them co-presenting with recurrent polyserositis
by: Carlos Córdova-Fletes, et al.
Published: (2020)

Blau syndrome complicated by granulomatous tubulointerstitial nephritis and immune complex mediated glomerulonephritis: A case report and review of the literature
by: Kelly M. Garrity, et al.
Published: (2024)

A Novel Variant in the Desmoplakin Gene in One Case of the Rare Carvajal Syndrome with Dilated Cardiomyopathy: A Case Report and Literature Review
by: Zhao XJ, et al.
Published: (2023)

Restrictive Cardiomyopathy in a Child
by: Shan-Miao Lin, et al.
Published: (2008)

Maternal and fetal outcomes in pregnant women with Takayasu aortoarteritis: Does optimally timed intervention in women with renal artery involvement improve pregnancy outcome?
by: Nilanchali Singh, et al.
Published: (2015)

Blau Syndrome: Report of a Rare Entity with Congenital Ostium Secundum Atrial Septal Defect in a 7-year-old Chinese Girl
by: Xian-hong Yang, et al.
Published: (2019)

Co-existence of Blau syndrome and NAID? Diagnostic challenges associated with presence of multiple pathogenic variants in NOD2 gene: a case report
by: Magdalena Dziedzic, et al.
Published: (2017)

The use of neurophysiological tests in integrated diagnostics of the myofascial pain syndrome in athletes
by: Z.M. Ostapyiak, et al.
Published: (2019)

Immunopharmacology of ulipristal as an emergency contraceptive
by: Miech RP
Published: (2011)

Tiim
by: RP Shankar
Published: (2007)

Factors influencing nurses' job satisfaction in selected private hospitals in England
by: RP Lephalala
Published: (2008)

Dilated cardiomyopathy with Graves disease in a young child
by: Yu Jung Choi, et al.
Published: (2016)

Adenomyoepithelioma of breast
by: S Pradhan, et al.
Published: (2011)