Néolithique -- Balkans -- Congrès. : Living well together? : settlement and materiality in the Neolithic of south-east and central Europe / edited by Douglass W. Bailey, Alasdair Whittle and Daniela Hofmann
2008
1
Néolithique -- Égée, Mer (région) : Prehistoric textiles : the development of cloth in the Neolithic and Bronze Ages with special reference to the Aegean / by E.J.W. Barber
1992
1
Néolithique -- Europe centrale -- Congrès. : Living well together? : settlement and materiality in the Neolithic of south-east and central Europe / edited by Douglass W. Bailey, Alasdair Whittle and Daniela Hofmann
2008
1
Néolithique -- Grande-Bretagne -- Avebury. : The harmony of symbols : the Windmill Hill causewayed enclosure, Wiltshire / by Alasdair Whittle, Joshua Pollard and Caroline Grigson ; with contributions by Janet Ambers [and others]
1999
1
Néolithique -- Moyen-Orient. : Quaternary of the Levant : environments, climate change, and humans / edited by Yehouda Enzel and Ofer Bar-Yosef
2017
1
Néolithique -- Turquie -- Congrès. : Living well together? : settlement and materiality in the Neolithic of south-east and central Europe / edited by Douglass W. Bailey, Alasdair Whittle and Daniela Hofmann
Fetal and neonatal addiction and withdrawal as a result of the mother's dependence on drugs during pregnancy. Withdrawal or abstinence symptoms develop shortly after birth. Symptoms exhibited are loud, high-pitched crying, sweating, yawning and gastrointestinal disturbances
A heterogeneous group of inherited metabolic disorders marked by absent or dysfunctional PEROXISOMES. Peroxisomal enzymatic abnormalities may be single or multiple. Biosynthetic peroxisomal pathways are compromised, including the ability to synthesize ether lipids and to oxidize long-chain fatty acid precursors. Diseases in this category include ZELLWEGER SYNDROME; INFANTILE REFSUM DISEASE; rhizomelic chondrodysplasia (CHONDRODYSPLASIA PUNCTATA, RHIZOMELIC); hyperpipecolic acidemia; neonatal adrenoleukodystrophy; and ADRENOLEUKODYSTROPHY (X-linked). Neurologic dysfunction is a prominent feature of most peroxisomal disorders
A heterogeneous group of inherited metabolic disorders marked by absent or dysfunctional PEROXISOMES. Peroxisomal enzymatic abnormalities may be single or multiple. Biosynthetic peroxisomal pathways are compromised, including the ability to synthesize ether lipids and to oxidize long-chain fatty acid precursors. Diseases in this category include ZELLWEGER SYNDROME; INFANTILE REFSUM DISEASE; rhizomelic chondrodysplasia (CHONDRODYSPLASIA PUNCTATA, RHIZOMELIC); hyperpipecolic acidemia; neonatal adrenoleukodystrophy; and ADRENOLEUKODYSTROPHY (X-linked). Neurologic dysfunction is a prominent feature of most peroxisomal disorders
A genus of REOVIRIDAE, causing acute gastroenteritis in BIRDS and MAMMALS, including humans. Transmission is horizontal and by environmental contamination. Seven species (Rotaviruses A thru G) are recognized
Diseases of newborn infants present at birth (congenital) or developing within the first month of birth. It does not include hereditary diseases not manifesting at birth or within the first 30 days of life nor does it include inborn errors of metabolism. Both HEREDITARY DISEASES and METABOLISM, INBORN ERRORS are available as general concepts
