Familial idiopathic hypercalciuria

Familial idiopathic hypercalciuria

Saved in:

Bibliographic Details
Main Authors:	N Buyan, U Saatçi, A Bakkaloğlu, N Beşbaş
Format:	Article
Language:	English
Published:	Hacettepe University Institute of Child Health 1988-07-01
Series:	The Turkish Journal of Pediatrics
Online Access:	https://turkjpediatr.org/article/view/3886
Tags:	Add Tag No Tags, Be the first to tag this record!

Similar Items

Amyloidosis in children with familial Mediterranean fever
by: H Koçak, et al.
Published: (1989-10-01)

Familial focal segmental glomerulosclerosis in infancy
by: A Bakkaloğlu, et al.
Published: (1988-01-01)

Hypercalciuria and nephrocalcinosis in cystic fibrosis patients
by: Uğur Ozçelik, et al.
Published: (2004-01-01)

The Vitamin D Metabolite Diagnostic Ratio Associates With Phenotypic Traits of Idiopathic Hypercalciuria
by: Nasser A. Dhayat, et al.
Published: (2024-04-01)

The Implications of the Vitamin D Metabolite Diagnostic Ratio in the Assessment of Patients With Idiopathic Hypercalciuria
by: Augusto Cesar Soares dos Santos Junior, et al.
Published: (2024-04-01)

Efficacy of oxybutynin, pseudoephedrine and indomethacin in the treatment of primary nocturnal enuresis
by: B Varan, et al.
Published: (1996-04-01)

Peripheral arterial thrombosis in systemic lupus erythematosis and nephrotic syndrome: possible association with protein S deficiency
by: N Beşbaş, et al.
Published: (1997-01-01)

Hypercalciuria in Children with Monosymptomatic Nocturnal Enuresis
by: Mahmut Çivilibal, et al.
Published: (2014-03-01)

Nephrocalcinosis due to vitamin D intoxication
by: N Beşbaş, et al.
Published: (1989-07-01)

METABOLIC ALKALEMIA IN HYPERCALCIURIA STONE FORMERS: DOES IT MATTER?
by: Renato V. M. Starek, et al.
Published: (2024-10-01)

Soft tissue calcification in chronic renal failure in childhood
by: U Saatçi, et al.
Published: (1982-10-01)

Identification of modifier gene variants overrepresented in familial hypomagnesemia with hypercalciuria and nephrocalcinosis patients with a more aggressive renal phenotype.
by: Monica Vall-Palomar, et al.
Published: (2025-04-01)

Hypomagnesemia-hypercalciuria-nephrocalcinosis and ocular findings: a new claudin-19 mutation
by: Zelal Ekinci, et al.
Published: (2012-04-01)

Assessment of bone status and bone turnover in pediatric patients with familiar hypomagnesemia with hypercalciuria and nephrocalcinosis
by: Beata Bieniaś, et al.
Published: (2025-05-01)

Biochemical markers of bone turnover in the diagnosis of renal osteodystrophy in dialyzed children
by: Esra Baskin, et al.
Published: (2004-01-01)

Autosomal dominant hypercalciuria in a mouse model due to a mutation of the epithelial calcium channel, TRPV5.
by: Nellie Y Loh, et al.
Published: (2013-01-01)

Autosomal recessive polycystic kidney disease: mapping to chromosomal region of 6p21-cen in a Turkish child
by: N Beşbaş, et al.
Published: (1998-04-01)

Hereditary Hypophosphatemic Rickets with Hypercalciuria (HHRH) Presenting with Genu Valgum Deformity: Treatment with Phosphate Supplementation and Surgical Correction
by: Juan M. Colazo, et al.
Published: (2020-01-01)

Calcium-sensing receptor and aquaporin 2 interplay in hypercalciuria-associated renal concentrating defect in humans. An in vivo and in vitro study.
by: Giuseppe Procino, et al.
Published: (2012-01-01)

Novel Variant of SLC34A3 in a Compound Heterozygous Brazilian Girl with Hereditary Hypophosphatemic Rickets with Hypercalciuria
by: Luciana Pinto Valadares, et al.
Published: (2025-09-01)

Investigating the Prevalence of Hypercalciuria in Children Aged 2–16 Years With Asymptomatic Microscopic Hematuria in 2020 in Tehran Children's Medical Center
by: Izat MohammadKhawajah, et al.
Published: (2024-11-01)

Newly identified intronic and known pathogenic point mutations in SLC34A3/NPT2c cause hereditary hypophosphatemic rickets with hypercalciuria
by: Yujing Sun, et al.
Published: (2025-03-01)

The Relationship between Social Self and Family as an Institution in Ayfer Tunç’s Novels and Stories
by: Şeyma Bakkaloğlu
Published: (2021-06-01)

Severe iron deficiency anemia in a child with idiopathic pulmonary hemosiderosis: a case report
by: Murat Derbent, et al.
Published: (2002-07-01)

Familial hypercholesterolemia mimicking juvenile idiopathic arthritis
by: Pooja Dhaon, et al.
Published: (2022-01-01)

Diabetes mellitus, diabetes insipidus, optic atrophy and deafness (DIDMOAD syndrome)
by: U Saatçi, et al.
Published: (1990-07-01)

A rare case of familial symptomatic spontaneous idiopathic pneumoperitoneum
by: Christelle Destinval, et al.
Published: (2024-11-01)

Revealing a brain network endophenotype in families with idiopathic generalised epilepsy.
by: Fahmida A Chowdhury, et al.
Published: (2014-01-01)

Successful treatment of a childhood synovitis, acne, pustulosis, hyperostosis and osteitis (SAPHO) syndrome with subcutaneous methotrexate: A case report
by: Meltem Akçaboy, et al.
Published: (2017-04-01)

Anti-neutrophil cytoplasmic antibodies (ANCA) in serum and bronchoalveolar lavage fluids of cystic fibrosis patients and patients with idiopathic bronchiectasis
by: Nazan Cobanoğlu, et al.
Published: (2010-08-01)

Analysis of the modifying effects of SAA1, SAA2 and TNF-alpha gene polymorphisms on development of amyloidosis in FMF patients
by: Engin Yilmaz, et al.
Published: (2003-07-01)

Idiopathic pulmonary embolism in a case of severe family ANKRD26 thrombocytopenia
by: Jérôme Guison, et al.
Published: (2017-06-01)

Diagnostic value of renal studies with radioisotopes in the pediatric age group
by: G Erbengi, et al.
Published: (1974-04-01)

Idiopathic Pulmonary Haemorrhage, Is It Really Idiopathic?
by: Stefanie Louey, et al.
Published: (2025-06-01)

Primary Idiopathic Chylopericardium
by: Sonia N. Rao, et al.
Published: (2024-08-01)

AN INHERITANCE OF IDIOPATHIC CARDIAC CONDUCTION DISORDERS
by: S. S. Tretyakova, et al.
Published: (2014-10-01)

CLINICAL IMPORTANCE OF IDIOPATHIC MITRAL ANNULAR CALCIFICATION
by: N. S. Chipigina, et al.
Published: (2016-01-01)

The association of nephrotic syndrome and renal vein thrombosis: a clinicopathological analysis of eight pediatric patients
by: K Tinaztepe, et al.
Published: (1989-01-01)

A variant of idiopathic epilepsy: Clinical note
by: V. A. Karlov, et al.
Published: (2015-03-01)

Hypereosinophilic syndrome associated with idiopathic eosinophilic vasculitis
by: B. Subhani, et al.
Published: (2025-08-01)