نتایج جستجو برای: hypophosphatemia

تعداد نتایج: 1219  

Journal: :BMJ case reports 2017
Rimesh Pal Anil Bhansali

Pal R, Bhansali A. BMJ Case Rep 2017. doi:10.1136/bcr-2017-220920 Description A 42-year-old man presented with lower limb bowing since childhood along with low backache and proximal muscle weakness for 8 years. He had strong family history of similar complaints in his elder brother, younger sister and daughter. Examination revealed loss of teeth and genu varum. Investigations showed corrected s...

2016
Amir Hossein Jafari-Rouhi Kavous Shahsavarinia Zahra Motazedi Leila Mahmoudi Fatemeh Ahmadi Amir Ghafarzad

1 Assistant Professor, Road Traffic Injury Research Center, Tabriz University of Medical Sciences, Tabriz, Iran 2 Nursing Research Committee, Sina Hospital, Tabriz University of Medical Sciences, Tabriz, Iran 3 General Practitioner, Emergency Medicine Research Team, Tabriz University of Medical Sciences, Tabriz, Iran 4 Nursing Research Committee, Tabriz Children's Hospital, Tabriz University of...

Journal: :Chest 1997
R T Sankaran J Mattana S Pollack P Bhat T Ahuja A Patel P C Singhal

STUDY OBJECTIVES This study was undertaken to evaluate the laboratory abnormalities observed in patients with bacterial pneumonia as predictors of the severity of illness. DESIGN Retrospective analysis. SETTING Tertiary care hospital. PATIENTS AND PARTICIPANTS We studied 302 consecutive patients who were admitted to the Long Island Jewish Medical Center from January through December 1993 ...

Journal: :The Journal of clinical investigation 1995
R Kilav J Silver T Naveh-Many

Phosphate is central to bone metabolism and we have therefore studied whether parathyroid hormone (PTH) is regulated by dietary phosphate in vivo. Weanling rats were fed diets with different phosphate contents for 3 wk: low phosphate (0.02%), normal calcium (0.6%), normal phosphate (0.3%), and calcium (0.6%); high phosphate (1.2%), high calcium (1.2%). The low phosphate diet led to hypophosphat...

2015
Tong Meng Wang Zhou Bo Li Huabin Yin Zhenxi Li Lei Zhou Jinhai Kong Wangjun Yan Xinghai Yang Tielong Liu Dianwen Song Jianru Xiao

BACKGROUND Tumor-induced osteomalacia (TIO) is a rare disorder, which is commonly found in craniofacial locations and in the extremities. To the best of our knowledge, only 16 cases have been described in the spine, and this is the first report to describe a case of patient with TIO in the thoracic spine combined with a mesenchymal hamartoma which had confused the therapeutic strategies to date...

2010
Nathan A Wigner Hilary F Luderer Megan K Cox Karen Sooy Louis C Gerstenfeld Marie B Demay

Hypophosphatemia leads to rickets and osteomalacia, the latter of which results in decreased biomechanical integrity of bones, accompanied by poor fracture healing. Impaired phosphate-dependent apoptosis of hypertrophic chondrocytes is the molecular basis for rickets. However, the underlying pathophysiology of impaired fracture healing has not been characterized previously. To address the role ...

2011
Fang-Ke Hu Fang Yuan Cheng-Ying Jiang Da-Wei Lv Bei-Bei Mao Qiang Zhang Zeng-Qiang Yuan Yan Wang

Tumor-induced osteomalacia (TIO), or oncogenic osteomalacia (OOM), is a rare acquired paraneoplastic disease characterized by renal phosphate wasting and hypophosphatemia. Recent evidence shows that tumor-overexpressed fibroblast growth factor 23 (FGF23) is responsible for the hypophosphatemia and osteomalacia. The tumors associated with TIO are usually phosphaturic mesenchymal tumor mixed conn...

2015
W. Grünberg J.A. Mol E. Teske

BACKGROUND Hypophosphatemia in early lactating dairy cows has been implicated as primary cause for postparturient hemoglobinuria in cattle. Decreased availability of phosphorus has been proposed to reduce adenosine triphosphate synthesis of erythrocytes and thereby reduce osmotic resistance of these cells. HYPOTHESIS/OBJECTIVES To study the effect of phosphorus depletion on the phosphate conc...

2010
Outi Mäkitie Renata C Pereira Ilkka Kaitila Serap Turan Murat Bastepe Tero Laine Heikki Kröger William G Cole Harald Jüppner

Homozygous inactivating mutations in DMP1 (dentin matrix protein 1), the gene encoding a noncollagenous bone matrix protein expressed in osteoblasts and osteocytes, cause autosomal recessive hypophosphatemia (ARHP). Herein we describe a family with ARHP owing to a novel homozygous DMP1 mutation and provide a detailed description of the associated skeletal dysplasia and carrier phenotype. The tw...

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