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Herders -- Mongolia. : Morin khuur : the soul of the Mongolian horseman  2006 1
Herders -- Mongolia -- Biography. : Herdsman to statesman : the autobiography of Jamsrangiin Sambuu of Mongolia / introduced and edited by Morris Rossabi ; translated by Mary Rossabi  2010 1
Herders -- Mongolia -- History. : A history of land use in Mongolia : the thirteenth century to the present / Elizabeth Endicott  2012 1
Herders -- Mongolia -- Psychology. : Faces of the wolf : managing the human, non-human boundary in Mongolia / by Bernard Charlier  2015 1
Herders -- Nepal -- Malemchigāon. : Himalayan herders / Naomi H. Bishop  1998 1
Herders -- Nepal -- Melemchi : Himalayan herders / Naomi H. Bishop  1998 1
Herders -- New Caledonia. : Overseas legends. The stockmen of “Grand Caillou” / directed by Jérôme Segur  1996 1
Herders -- Northern Territory -- History : End of an era : Aboriginal labour in the Northern Territory / Ronald M. Berndt & Catherine H. Berndt  1987 1
Herders -- Peru -- Chillihuani : Growing up in a culture of respect : child rearing in highland Peru / Inge Bolin  2006 1
Herders -- Social life and customs. : Morin Khuur: The Soul Of The Mongolian Horseman / Director: Segur, Benoit  2011 1
Herders -- Thailand. : Stories from the north / directed by Uruphong Raksasad  2006 1
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  1988 1
  Herding -- 4 Related Subjects   4
Herding. : MythBusters: Herding Cats/Full of Crap/Greased Pig - Ep 221 / Director: Christiansen, Steve  2014 1
Herding -- Africa. : Pastoralism in Africa : past, present, and futures / edited by Michael Bollig, Michael Schnegg and Hans-Peter Wotzka  2013 1
Herding -- Africa -- History. : Pastoralism in Africa : past, present, and futures / edited by Michael Bollig, Michael Schnegg and Hans-Peter Wotzka  2013 1
Herding -- Alaska, Northwest -- History. : Caribou herds of northwest Alaska, 1850-2000 / by Ernest S. Burch Jr. ; edited by Igor Krupnik and Jim Dau  2012 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


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Herding -- Mongolia.   2
 

Herding systems -- See Pastoral systems


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Herdsmen -- See Herders


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Here and now with watchers (Choreographic work : Hawkins) : Erick Hawkins - poet of the modern dance : speaking of dance / American Dance Festival Video ; directed and produced by Douglas Rosenberg  1995 1
 

Here beginneth a mery geste of Robyn Hode and his meyne -- See Lytell geste of Robyn Hode


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Here begynnys the tale of Syr Eglamoure of Artoys -- See Sir Eglamour of Artois


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Hērē (Greek deity) -- See Hera (Greek deity)


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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  2006 1
 

Herebertus, Bosehamensis, active 12th century -- See Herbert, of Bosham, active 12th century


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Heredia, Alberto Baltazar Urista -- See Alurista


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Heredia, José-Maria de, 1842-1905. Trophees : Trophies : taken mostly from the French of Jose Maria de Heredia / by Martin Haley  1972? 1
 

Heredia, José Antonio Primo de Rivera y Sáenz de, 1903-1936 -- See Primo de Rivera, José Antonio, 1903-1936


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Heredia, José-Maria de, 1842-1905. Trophees : Trophies : taken mostly from the French of Jose Maria de Heredia / by Martin Haley  1972? 1
 

Heredia, José-Marie de, 1842-1905 -- See Heredia, José-Maria de, 1842-1905


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Hereditary ataxia -- See Friedreich's ataxia


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Hereditary Ataxia, Friedreich -- See Friedreich Ataxia


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)
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Hereditary Ataxia, Friedreich's -- See Friedreich Ataxia


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)
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Hereditary Ataxias, Friedreich's -- See Friedreich Ataxia


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)
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Hereditary Blood Coagulation Disorders -- See Blood Coagulation Disorders, Inherited


Hemorrhagic and thrombotic disorders that occur as a consequence of inherited abnormalities in blood coagulation
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Hereditary Breast and Ovarian Cancer Syndrome -- genetics. : Waiting for Cancer to Come : Women's Experiences with Genetic Testing and Medical Decision Making for Breast and Ovarian Cancer / Sharlene Hesse-Biber  2014 1
 

Hereditary Cancer Syndrome -- See Neoplastic Syndromes, Hereditary


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
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Hereditary Cancer Syndromes -- See Neoplastic Syndromes, Hereditary


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
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Hereditary Central Nervous System Demyelinating Diseases. : Bioimaging in neurodegeneration / edited by Patricia A. Broderick, David N. Rahni, Edwin H. Kolodny  2005 1
  Hereditary Chorea -- 2 Related Subjects   2
 

Hereditary Chorea, Benign -- See Chorea


Involuntary, forcible, rapid, jerky movements that may be subtle or become confluent, markedly altering normal patterns of movement. Hypotonia and pendular reflexes are often associated. Conditions which feature recurrent or persistent episodes of chorea as a primary manifestation of disease are referred to as CHOREATIC DISORDERS. Chorea is also a frequent manifestation of BASAL GANGLIA DISEASES
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Hereditary Choreas -- See Chorea


Involuntary, forcible, rapid, jerky movements that may be subtle or become confluent, markedly altering normal patterns of movement. Hypotonia and pendular reflexes are often associated. Conditions which feature recurrent or persistent episodes of chorea as a primary manifestation of disease are referred to as CHOREATIC DISORDERS. Chorea is also a frequent manifestation of BASAL GANGLIA DISEASES
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Hereditary Choreas, Benign -- See Chorea


Involuntary, forcible, rapid, jerky movements that may be subtle or become confluent, markedly altering normal patterns of movement. Hypotonia and pendular reflexes are often associated. Conditions which feature recurrent or persistent episodes of chorea as a primary manifestation of disease are referred to as CHOREATIC DISORDERS. Chorea is also a frequent manifestation of BASAL GANGLIA DISEASES
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Hereditary Coagulation Disorder -- See Blood Coagulation Disorders, Inherited


Hemorrhagic and thrombotic disorders that occur as a consequence of inherited abnormalities in blood coagulation
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Hereditary Coagulation Disorders -- See Blood Coagulation Disorders, Inherited


Hemorrhagic and thrombotic disorders that occur as a consequence of inherited abnormalities in blood coagulation
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Hereditary Corneal Dystrophies -- See Corneal Dystrophies, Hereditary


Bilateral hereditary disorders of the cornea, usually autosomal dominant, which may be present at birth but more frequently develop during adolescence and progress slowly throughout life. Central macular dystrophy is transmitted as an autosomal recessive defect
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