Here are entered collections of secular, or sacred and secular, musical works in which spoken language is an integral part. Individual secular works and collections for a specific medium of performance are entered under the heading followed by the medium. The medium "instrumental ensemble" stands for two or more different solo instruments; "voice" for a solo voice of high, low, or medium range; and "chorus" for men's, mixed, women's, or children's voices in two or more parts. Collections of sacred musical works in which spoken language is an integral part are entered under Sacred monologues with music
Récits de voyages -- 13e siècle. : The mission of Friar William of Rubruck : his journey to the court of the Great Khan Möngke, 1253-1255 / translated by Peter Jackson ; introduction, notes and appendices by Peter Jackson with David Morgan
Récits de voyages chinois -- Anthologies. : Inscribed landscapes : travel writing from imperial China / translated with annotations and an introduction by Richard E. Strassberg
Récits d'horreurs anglais. : Sisters of Gore : seven Gothic melodramas by British women, 1790-1843 / edited with introductions and notes by John Franceschina
Russie -- Politique et gouvernement -- 1894-1917 -- Récits personnels. : The making of three Russian revolutionaries : voices from the Menshevik past / Leopold H. Haimson in collaboration with Ziva Galili y Garcia and Richard Wortman ; introduction by Leopold H. Haimson ; notes by Ziva Galili y Garcia
Shoah -- Pologne -- Récits personnels. : A surplus of memory : chronicle of the Warsaw Ghetto uprising / Yitzhak Zuckerman ("Antek") ; translated and edited by Barbara Harshav
Recke, Elisa von der, 1754-1833 -- Congresses : Elisa von der Recke : aufklärerische Kontexte und lebensweltliche Perspektiven / herausgegeben von Valerie Leyh, Adelheid Müller, Vera Viehöver
An autosomal dominant inherited disorder (with a high frequency of spontaneous mutations) that features developmental changes in the nervous system, muscles, bones, and skin, most notably in tissue derived from the embryonic NEURAL CREST. Multiple hyperpigmented skin lesions and subcutaneous tumors are the hallmark of this disease. Peripheral and central nervous system neoplasms occur frequently, especially OPTIC NERVE GLIOMA and NEUROFIBROSARCOMA. NF1 is caused by mutations which inactivate the NF1 gene (GENES, NEUROFIBROMATOSIS 1) on chromosome 17q. The incidence of learning disabilities is also elevated in this condition. (From Adams et al., Principles of Neurology, 6th ed, pp1014-18) There is overlap of clinical features with NOONAN SYNDROME in a syndrome called neurofibromatosis-Noonan syndrome. Both the PTPN11 and NF1 gene products are involved in the SIGNAL TRANSDUCTION pathway of Ras (RAS PROTEINS)
