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)
The condition of a pattern of malignancies within a family, but not every individual's necessarily having the same neoplasm. Characteristically the tumor tends to occur at an earlier than average age, individuals may have more than one primary tumor, the tumors may be multicentric, usually more than 25 percent of the individuals in direct lineal descent from the proband are affected, and the cancer predisposition in these families behaves as an autosomal dominant trait with about 60 percent penetrance
The condition of a pattern of malignancies within a family, but not every individual's necessarily having the same neoplasm. Characteristically the tumor tends to occur at an earlier than average age, individuals may have more than one primary tumor, the tumors may be multicentric, usually more than 25 percent of the individuals in direct lineal descent from the proband are affected, and the cancer predisposition in these families behaves as an autosomal dominant trait with about 60 percent penetrance
