Reconstruction of deficits in long bones has always been a complicated and difficult
problem. Historically, amputation often was the only solution after extensive traumatic bone …

Abstract Neurofibromatosis type 1 (NF‐1) is an autosomal dominant disease that affects 1 in
3,000 persons worldwide. Café‐au‐lait macules and peripheral nerve sheath tumors (ie …

A strong relationship between congenital pseudarthrosis of the tibia (CPT) and
neurofibromatosis type 1 (NF1) has been suggested, but prevalence varies widely …

Calcium phosphate‐based bone substitutes have not been used to repair load‐bearing
bone defects due to their weak mechanical property. In this study, we reevaluated the …

Neurofibromatosis type 1 (NF1) or von Recklinghausen disease is one of the most common
autosomal dominant genetic diseases. It is characterized by 'café-au-lait'spots and multiple …

Background Reconstruction of large skeletal defects secondary to osteomyelitis or open
fracture is a challenging problem. The purpose of this study was to evaluate the results of …

Background. Neurofibromatosis Type 1 (NF‐1) has a variety of associated orthopaedic
manifestations that have been previously reported. We report a case of severe, grade 4 knee …

Уро ђе на псе у до ар тро за пот ко ле ни це убра ја се у нај ве ће иза зо ве у деч јој ор
то пе ди ји. Ин ци ден ци ја ове рет ке бо ле сти је све га 4–7 обо ле лих на ми ли он но …

Neurofibromatosis is an autosomal dominant disease which can be categorized into 3
subtypes: 1-NF1 2-NF2 3-schwannoma. This disease is a type of familial predisposition …

There have indeed been 2 previous studies comparing the types of fusion applied to a
particular type of listhesis but not spondylolisthesis in general. There might have been an …