The complete writings of Walt Whitman. Issued under the editorial supervision of his literary executors, Richard Maurice Bucke, Thomas B. Harned, and Horace L. Traubel;

"The book-lover's Camden edition."

Catalogue of important letters, manuscripts and books by or relating to Walt Whitman, the property of his intimate friend, biographer and literary executor, the late Richard Maurice Bucke of London, Ontario (sold by order of H. L. Bucke, esq.) which will be sold by auction by Messrs. Sotheby & co. ... the 13th of May, 1935.

117 lots.

Leaves of grass,

"Variorum readings of 'Leaves of grass', ed. by Oscar Lovell Triggs, PH.D.": v. 3, p. [83]-[255]

Une méthode dangereuse : comprendre le processus créateur en musique de film, le cas de Norman McLaren et Maurice Blackburn, David Cronenberg et Howard Shore

Cette version de la thèse a été tronquée des certains éléments protégés par le droit d’auteur. Une version plus complète est disponible en ligne pour les membres de la communauté de l’Université de Montréal et peut aussi être consultée dans une des bibliothèques UdeM.

The life and death of Richard Yea-and-Nay,

bk. I. The book of Yea.--bk. II. The book of Nay.

The life and death of Richard Yea-and-Nay /

Mode of access: Internet.

The life and death of Richard Yea-and-Nay /

Bk. I. The book of Yea.--Bk. II. The book of Nay.

L'art de diriger l'orchestre. Richard Wagner et Hans Richter, la neuvième symphonie.

"Les pages qui suivent ont d'abord paru dans Le guide musical": p. [5]

The plays of Maurice Maeterlinck

First series "limited to six hundred copies."

Updated Clinical Classification of Pulmonary Hypertension

The aim of a clinical classification of pulmonary hypertension (PH) is to group together different manifestations of disease sharing similarities in pathophysiologic mechanisms, clinical presentation, and therapeutic approaches. In 2003, during the 3rd World Symposium on Pulmonary Hypertension, the clinical classification of PH initially adopted in 1998 during the 2nd World Symposium was slightly modified. During the 4th World Symposium held in 2008, it was decided to maintain the general architecture and philosophy of the previous clinical classifications. The modifications adopted during this meeting principally concern Group 1, pulmonary arterial hypertension (PAH). This subgroup includes patients with PAH with a family history or patients with idiopathic PAH with germline mutations (e. g., bone morphogenetic protein receptor-2, activin receptor-like kinase type 1, and endoglin). In the new classification, schistosomiasis and chronic hemolytic anemia appear as separate entities in the subgroup of PAH associated with identified diseases. Finally, it was decided to place pulmonary venoocclusive disease and pulmonary capillary hemangiomatosis in a separate group, distinct from but very close to Group 1 (now called Group 1`). Thus, Group 1 of PAH is now more homogeneous. (J Am Coll Cardiol 2009;54:S43-54) (C) 2009 by the American College of Cardiology Foundation