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Dysfunctional families -- Rehabilitation. : 7.30: 24/02/16  2016 1
Dysfunctional families -- Services for.   15
Dysfunctional families -- Services for -- Addresses, esays, lectures : Child sexual abuse within the family / Ciba Foundation ; edited by Ruth Porter  1984 1
Dysfunctional families -- Services for -- Australia.   5
Dysfunctional families -- Services for -- Australia -- Victoria. : The Gordoncare Parent Orders Program : an evaluation / Thea Brown with Sarina Smale  2007 1
Dysfunctional families -- Services for -- Australia -- Victoria -- Evaluation. : The Gordoncare Parent Orders Program : an evaluation / Thea Brown with Sarina Smale  2007 1
Dysfunctional families -- Services for -- Case studies. : Child sexual abuse within the family / Ciba Foundation ; edited by Ruth Porter  1984 1
Dysfunctional families -- Services for -- Congresses.   2
Dysfunctional families -- Services for -- Great Britain.   4
Dysfunctional families -- Services for -- Moral and ethical aspects -- Congresses : Enfants à protéger, parents à aider [ressource électronique] : deux univers à rapprocher / sous la direction de Claire Chamberland, Sophie Léveillé, Nico Trocmé  2007 1
Dysfunctional families -- Services for -- Québec (Province)   2
Dysfunctional families -- Services for -- United States.   6
Dysfunctional families -- United States.   11
Dysfunctional families -- United States -- Case studies. : Complicated lives : girls, parents, drugs, and juvenile justice / Vera Lopez  2017 1
Dysfunctional families -- United States -- Case studies -- Comic books, strips, etc : Hey, kiddo : how I lost my mother, found my father, and dealt with family addiction / by Jarrett J. Krosoczka  2018 1
Dysfunctional families -- United States -- Cross-cultural studies.   2
Dysfunctional families -- United States -- Drama   5
Dysfunctional families -- United States -- Psychological aspects -- Juvenile literature. : Coping in a dysfunctional family / Raymond M. Jamiolkowski  1993 1
Dysfunctional families -- Victoria -- Melbourne -- Case studies : Fragmented lives / John Embling  1986 1
 

Dysfunctions, Central Auditory -- See Auditory Diseases, Central


Disorders of hearing or auditory perception due to pathological processes of the AUDITORY PATHWAYS in the CENTRAL NERVOUS SYSTEM. These include CENTRAL HEARING LOSS and AUDITORY PERCEPTUAL DISORDERS
  1
 

Dysfunctions, Cognitive -- See Cognitive Dysfunction


Diminished or impaired mental and/or intellectual function
  1
 

Dysfunctions, Communicative -- See Communication Disorders


Disorders of verbal and nonverbal communication caused by receptive or expressive LANGUAGE DISORDERS, cognitive dysfunction (e.g., MENTAL RETARDATION), psychiatric conditions, and HEARING DISORDERS
  1
 

Dysfunctions, General Peroxisomal -- See 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
  1
 

Dysfunctions, Left Ventricular -- See Ventricular Dysfunction, Left


A condition in which the LEFT VENTRICLE of the heart was functionally impaired. This condition usually leads to HEART FAILURE; MYOCARDIAL INFARCTION; and other cardiovascular complications. Diagnosis is made by measuring the diminished ejection fraction and a depressed level of motility of the left ventricular wall
  1
 

Dysfunctions, Liver -- See Liver Diseases


Pathological processes of the LIVER
  1
 

Dysfunctions, Multiple Peroxisomal -- See 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
  1
 

Dysfunctions, Neurologic -- See Neurologic Manifestations


Clinical signs and symptoms caused by nervous system injury or dysfunction
  1
 

Dysfunctions, Proteostasis -- See Proteostasis Deficiencies


Disorders caused by imbalances in the PROTEIN HOMEOSTASIS network - synthesis, folding, and transport of proteins; post-translational modifications; and degradation or clearance of misfolded proteins
  1
 

Dysfunctions, Psychological Sexual -- See Sexual Dysfunctions, Psychological


Disturbances in sexual desire and the psychophysiologic changes that characterize the sexual response cycle and cause marked distress and interpersonal difficulty. (APA, DSM-IV, 1994)
  1
 

Dysfunctions, Psychosexual -- See Sexual Dysfunctions, Psychological


Disturbances in sexual desire and the psychophysiologic changes that characterize the sexual response cycle and cause marked distress and interpersonal difficulty. (APA, DSM-IV, 1994)
  1
 

Dysfunctions, Right Ventricular -- See Ventricular Dysfunction, Right


A condition in which the RIGHT VENTRICLE of the heart was functionally impaired. This condition usually leads to HEART FAILURE or MYOCARDIAL INFARCTION, and other cardiovascular complications. Diagnosis is made by measuring the diminished ejection fraction and a depressed level of motility of the right ventricular wall
  1
 

Dysfunctions, Single Peroxisomal -- See 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
  1
 

Dysgenesis Neuroepithelialis Retinae -- See Leber Congenital Amaurosis


A rare degenerative inherited eye disease that appears at birth or in the first few months of life that results in a loss of vision. Not to be confused with LEBER HEREDITARY OPTIC NEUROPATHY, the disease is thought to be caused by abnormal development of PHOTORECEPTOR CELLS in the RETINA, or by the extremely premature degeneration of retinal cells
  1
 

Dysgeusia -- See Taste disorders


  1
 

Dysglossia -- See Speech Disorders


Acquired or developmental conditions marked by an impaired ability to comprehend or generate spoken forms of language
  1
 

Dysglossias -- See Speech Disorders


Acquired or developmental conditions marked by an impaired ability to comprehend or generate spoken forms of language
  1
  Dysgraphia -- 2 Related Subjects   2
 

Dysgraphia, Acquired -- See Agraphia


Loss or impairment of the ability to write (letters, syllables, words, or phrases) due to an injury to a specific cerebral area or occasionally due to emotional factors. This condition rarely occurs in isolation, and often accompanies APHASIA. (From Adams et al., Principles of Neurology, 6th ed, p485; APA, Thesaurus of Psychological Index Terms, 1994)
  1
 

Dysgraphia, Developmental -- See Agraphia


Loss or impairment of the ability to write (letters, syllables, words, or phrases) due to an injury to a specific cerebral area or occasionally due to emotional factors. This condition rarely occurs in isolation, and often accompanies APHASIA. (From Adams et al., Principles of Neurology, 6th ed, p485; APA, Thesaurus of Psychological Index Terms, 1994)
  1
 

Dysgraphias -- See Agraphia


Loss or impairment of the ability to write (letters, syllables, words, or phrases) due to an injury to a specific cerebral area or occasionally due to emotional factors. This condition rarely occurs in isolation, and often accompanies APHASIA. (From Adams et al., Principles of Neurology, 6th ed, p485; APA, Thesaurus of Psychological Index Terms, 1994)
  1
 

Dysgraphias, Acquired -- See Agraphia


Loss or impairment of the ability to write (letters, syllables, words, or phrases) due to an injury to a specific cerebral area or occasionally due to emotional factors. This condition rarely occurs in isolation, and often accompanies APHASIA. (From Adams et al., Principles of Neurology, 6th ed, p485; APA, Thesaurus of Psychological Index Terms, 1994)
  1
 

Dysgraphias, Developmental -- See Agraphia


Loss or impairment of the ability to write (letters, syllables, words, or phrases) due to an injury to a specific cerebral area or occasionally due to emotional factors. This condition rarely occurs in isolation, and often accompanies APHASIA. (From Adams et al., Principles of Neurology, 6th ed, p485; APA, Thesaurus of Psychological Index Terms, 1994)
  1
 

Dyskinesia -- See Movement disorders


  1
 

Dyskinesia, Ciliary -- See Ciliary Motility Disorders


Conditions caused by abnormal CILIA movement in the body, usually causing KARTAGENER SYNDROME, chronic respiratory disorders, chronic SINUSITIS, and chronic OTITIS. Abnormal ciliary beating is likely due to defects in any of the 200 plus ciliary proteins, such as missing motor enzyme DYNEIN arms
  1
  Dyskinesia, Drug-induced -- 2 Related Subjects   2
Dyskinesia, Drug-Induced.   2
Dyskinesia, Drug-Induced -- physiopathology. : Mechanisms of L-DOPA-induced dyskinesia in Parkinson's disease / Angela Cenci  2014 1
Dyskinesia, Drug-Induced -- prevention & control. : Promising medical therapies for Parkinson's disease / Robert A. Hauser  2014 1
Dyskinesia, Drug-Induced -- therapy. : Mechanisms of L-DOPA-induced dyskinesia in Parkinson's disease / Angela Cenci  2014 1
 

Dyskinesia, Medication-Induced -- See Dyskinesia, Drug-Induced


Abnormal movements, including HYPERKINESIS; HYPOKINESIA; TREMOR; and DYSTONIA, associated with the use of certain medications or drugs. Muscles of the face, trunk, neck, and extremities are most commonly affected. Tardive dyskinesia refers to abnormal hyperkinetic movements of the muscles of the face, tongue, and neck associated with the use of neuroleptic agents (see ANTIPSYCHOTIC AGENTS). (Adams et al., Principles of Neurology, 6th ed, p1199)
  1
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