OPERATIONS FOR STONE, BY MR. COSTELLO.
نویسندگان
چکیده
منابع مشابه
Costello syndrome.
Costello syndrome is a rare, distinctive, multiple congenital anomaly syndrome, characterized by soft, loose skin with deep palmar and plantar creases, loose joints, distinctive coarse facial features and skeletal and cardiac abnormalities. The affected patients have a predisposition to develop malignancy, developmental delays and mental retardation. Recently, a 7-year-old male child born to no...
متن کاملErrata list for "Error Control Coding" by Lin and Costello
This documents lists some errors found in the second edition of Error Control Coding by Shu Lin and Daniel J. Costello.
متن کاملDr. Joseph Fayrer on Stone Operations in 1865
a casual reference to the authority, practice or opinion of any Indian Surgeon. "Take lithotomy for example, the fullest and most elaborate details are quoted of the practice of British and Continental Surgeons, yet not a word on the subject relates to India, where some of our graduates have cut as many men successfully for stone as the greatest lithotomists Europe ever saw. ... I might refer t...
متن کاملKEVIN COSTELLO Definition
This is the first of two papers which construct a purely algebraic counterpart to the theory of Gromov-Witten invariants (at all genera). These GromovWitten type invariants depend on a Calabi-Yau A∞ category, which plays the role of the target in ordinary Gromov-Witten theory. When the Fukaya category of a compact symplectic manifold X is used, it is shown, under certain assumptions, that the u...
متن کاملAnaesthetic Management in Costello Syndrome.
Costello syndrome is a rare genetic disorder characterised by growth and mental retardation, macrocephaly, short neck and macroglossia. Cardiac involvement can also occur in Costello syndrome and is presented in the form of hypertrophic cardiomyopathy, tachyarrythmias and valvular dysfunction. Nervous system involvement including ventriculomegaly, hydrocephaly and Chiari type 1 malformation are...
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ژورنال
عنوان ژورنال: The Lancet
سال: 1837
ISSN: 0140-6736
DOI: 10.1016/s0140-6736(02)82132-8