Results 101 to 110 of about 1,505 (162)

Etiology and longitudinal kidney outcomes in children with nephrocalcinosis: a retrospective cohort study. [PDF]

Front Pediatr
İnözü M, Şenses SÇ, Aksoy ÖY, Yazıcıoğlu B, Özlü SG, Çaycı FŞ, Bayrakçı US.   +6 more
europepmc   +1 more source

A Case Report: Familial Hypophosphatemic Vitamin D Resistant Rickets.

, 1991
Hisanao Tahara, Osamu Yamada, Yuichi Ishibashi, Isao Saikawa, Tomoki Ishizaki, Ken Kusaba, Akira Okue, Nobuyuki Matsuguchi   +7 more
core   +1 more source

Nephrocalcinosis: unveiling renal tubulopathies in the genomic era. [PDF]

J Bras Nefrol
Ayoub EAM, Vaisbich MH, Rocha DR, Cerqueira BP, Matos ACC, Pietrobom IG, Heilberg IP.   +6 more
europepmc   +1 more source

The impact of monoallelic inactivation mutations in the ENPP1 gene on pediatric skeletal development: a case report and literature review. [PDF]

Front Endocrinol (Lausanne)
Lu S, Sun N, Li Y, Wu Z, Zhang J.
europepmc   +1 more source

Peripheral Precocious Puberty Due to Autonomous Gonadal Activation: A Multicenter Experience. [PDF]

Cureus
Yewale S, Khadilkar V, Shah N, Mehta S, Prasad HK, Oza C, Kumbhojkar A, Deshpande R, Maheshwari A, Khadilkar A.   +9 more
europepmc   +1 more source

Iron-Induced Hypophosphatemia: A Review of Pathophysiology, Drug Safety, and Pharmacogenomic Perspectives. [PDF]

J Hematol
Pozzessere S.
europepmc   +1 more source

The Diagnosis and Therapy of XLH. [PDF]

Calcif Tissue Int
Böckmann I, Haffner D.
europepmc   +1 more source

Advancing patient evidence in XLH (APEX): rationale and design of a real-world XLH global data unification program. [PDF]

Front Endocrinol (Lausanne)
Brandi ML, Carpenter TO, Fukumoto S, Haffner D, Imel EA, Kanematsu M, McCullough KP, Ozono K.   +7 more
europepmc   +1 more source

Dental Manifestations in Children Affected by Hypophosphatemic Rickets: A Systematic Review and Meta-Analysis. [PDF]

Children (Basel)
Allam A, Cirio S, Elia F, Salerno C, Cagetti MG.   +4 more
europepmc   +1 more source

Phenotypic characterization of ENPP1 deficiency: generalized arterial calcification of infancy and autosomal recessive hypophosphatemic rickets type 2. [PDF]

JBMR Plus
Ferreira CR, Hackbarth ME, Nitschke Y, Botschen U, Gafni RI, Mughal MZ, Baujat G, Schnabel D, Schou IM, Khursigara G, Reardon O, Burklow TR, Swanner K, Rutsch F.   +13 more
europepmc   +1 more source