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3-hydroxy-7-(hydroxyimino)cholanic acid (HHCA)

Also Known As:

HHCA; LCA-7-oxime

Networked: 6 relevant articles (0 outcomes, 0 trials/studies)

Bio-Agent Context: Research Results

Polycyclic Compounds: 6
- Fused-Ring Compounds
  - Steroids: 70059
    - Bile Acids and Salts: 11432
      - Cholic Acids: 14
        3-hydroxy-7-(hydroxyimino)cholanic acid: 6
    - Cholanes
      - Cholic Acids: 14
        3-hydroxy-7-(hydroxyimino)cholanic acid: 6

Experts

1.	Auer, Timo Alexander: 1 article (06/2020)
2.	Bläker, Hendrik: 1 article (06/2020)
3.	Denecke, Timm: 1 article (06/2020)
4.	Fehrenbach, Uli: 1 article (06/2020)
5.	Geisel, Dominik: 1 article (06/2020)
6.	Grieser, Christian: 1 article (06/2020)
7.	Müller, Tobias: 1 article (06/2020)
8.	Penzkofer, Tobias: 1 article (06/2020)
9.	Schmelzle, Moritz: 1 article (06/2020)
10.	Seehofer, Daniel: 1 article (06/2020)

Related Diseases

1.	Cerebellar Ataxia (Dysmetria) 01/01/1994 - "HHCA and LCCA: cerebellar ataxia predominated in all stages, and neurological signs other than cerebellar ataxia were rare. " 12/01/1993 - "The percentage of patients with each subtype of SCD was; olivopontocerebellar atrophy (OPCA) 34.4%, Menzel type of hereditary cerebellar ataxia (MHCA) 12.6%, Holmes type of hereditary cerebellar ataxia (HHCA) 7.5%, Shy-Drager syndrome (SDS) 7.0%, hereditary spastic paraplegia (HSP) 3.9%, dentatorubro-pallidoluysian atrophy (DRPLA) 2.5%, Friedreich ataxia (FA) 2.4%, Joseph disease (JD) 2.0%, and striatonigral degeneration (SND) 1.5% in decreasing order. "
2.	Peripheral Arterial Disease 10/01/1996 - "Hyperhomocysteinaemia (HHCA) is established as an independent risk factor for coronary and peripheral arterial disease. "
3.	Striatonigral Degeneration 12/01/1993 - "The percentage of patients with each subtype of SCD was; olivopontocerebellar atrophy (OPCA) 34.4%, Menzel type of hereditary cerebellar ataxia (MHCA) 12.6%, Holmes type of hereditary cerebellar ataxia (HHCA) 7.5%, Shy-Drager syndrome (SDS) 7.0%, hereditary spastic paraplegia (HSP) 3.9%, dentatorubro-pallidoluysian atrophy (DRPLA) 2.5%, Friedreich ataxia (FA) 2.4%, Joseph disease (JD) 2.0%, and striatonigral degeneration (SND) 1.5% in decreasing order. "
4.	Hyperhomocysteinemia 01/01/2006 - "Hyperhomocysteinemia (HHCA) is defined as an independent risk factor for atherothrombotic vascular disease; therefore, screening for HHCA is recommended. "
5.	Multiple System Atrophy 12/01/1993 - "Similarity and differences in non-hereditary cerebellar form (LCCA, HHCA), multiple system atrophy (OPCA, SDS, SND), hereditary cerebello-brainstem form (MHCA, JD, DRPLA), and hereditary spinal from (FA, HSP) were elucidated. "

Related Therapies and Procedures

1.	Cardiopulmonary Bypass (Heart-Lung Bypass)