Herders -- Western Australia -- Kimberley -- Biography : Raparapa kularr martuwarra : all right, now we go 'side the river, along that sundown way, stories / from the Fitzroy River drovers, Eric Lawford ... [and others] ; edited by Paul Marshall
1988
1
Herders -- Western Australia -- Kimberley -- History : Raparapa kularr martuwarra : all right, now we go 'side the river, along that sundown way, stories / from the Fitzroy River drovers, Eric Lawford ... [and others] ; edited by Paul Marshall
Herding -- Balkan Peninsula -- History : Animal husbandry and hunting in the central and western Balkans through time / Nemanja Marković ; Jelena Bulatović
2020
1
Herding -- China -- Dege Xian : Nomads of eastern Tibet : social organization and economy of a pastoral estate in the kingdom of Dege / by Rinzin Thargyal ; edited by Toni Huber
2007
1
Herding dogs -- See Also the narrower term Sheep dogs
Myers, Walter Dean, 1937-2014. Here in Harlem : Literary newsmakers for students. Volume 1 : presenting analysis, context, and criticism on newsmaking novels, nonfiction, and poetry / Anne Marie Hacht, editor ; foreword by Greg Wilson
Heredia, José María, 1803-1839 -- Correspondence : José María Heredia in New York, 1823-1825 : an exiled Cuban poet in the age of revolution, selected letters and verse / edited, translated, and with an introduction by Frederick Luciani
Heredia, José María, 1803-1839 -- Translations : José María Heredia in New York, 1823-1825 : an exiled Cuban poet in the age of revolution, selected letters and verse / edited, translated, and with an introduction by Frederick Luciani
An autosomal recessive disease, usually of childhood onset, characterized pathologically by degeneration of the spinocerebellar tracts, posterior columns, and to a lesser extent the corticospinal tracts. Clinical manifestations include GAIT ATAXIA, pes cavus, speech impairment, lateral curvature of spine, rhythmic head tremor, kyphoscoliosis, congestive heart failure (secondary to a cardiomyopathy), and lower extremity weakness. Most forms of this condition are associated with a mutation in a gene on chromosome 9, at band q13, which codes for the mitochondrial protein frataxin. (From Adams et al., Principles of Neurology, 6th ed, p1081; N Engl J Med 1996 Oct 17;335(16):1169-75) The severity of Friedreich ataxia associated with expansion of GAA repeats in the first intron of the frataxin gene correlates with the number of trinucleotide repeats. (From Durr et al, N Engl J Med 1996 Oct 17;335(16):1169-75)
An autosomal recessive disease, usually of childhood onset, characterized pathologically by degeneration of the spinocerebellar tracts, posterior columns, and to a lesser extent the corticospinal tracts. Clinical manifestations include GAIT ATAXIA, pes cavus, speech impairment, lateral curvature of spine, rhythmic head tremor, kyphoscoliosis, congestive heart failure (secondary to a cardiomyopathy), and lower extremity weakness. Most forms of this condition are associated with a mutation in a gene on chromosome 9, at band q13, which codes for the mitochondrial protein frataxin. (From Adams et al., Principles of Neurology, 6th ed, p1081; N Engl J Med 1996 Oct 17;335(16):1169-75) The severity of Friedreich ataxia associated with expansion of GAA repeats in the first intron of the frataxin gene correlates with the number of trinucleotide repeats. (From Durr et al, N Engl J Med 1996 Oct 17;335(16):1169-75)
An autosomal recessive disease, usually of childhood onset, characterized pathologically by degeneration of the spinocerebellar tracts, posterior columns, and to a lesser extent the corticospinal tracts. Clinical manifestations include GAIT ATAXIA, pes cavus, speech impairment, lateral curvature of spine, rhythmic head tremor, kyphoscoliosis, congestive heart failure (secondary to a cardiomyopathy), and lower extremity weakness. Most forms of this condition are associated with a mutation in a gene on chromosome 9, at band q13, which codes for the mitochondrial protein frataxin. (From Adams et al., Principles of Neurology, 6th ed, p1081; N Engl J Med 1996 Oct 17;335(16):1169-75) The severity of Friedreich ataxia associated with expansion of GAA repeats in the first intron of the frataxin gene correlates with the number of trinucleotide repeats. (From Durr et al, N Engl J Med 1996 Oct 17;335(16):1169-75)
