apnea has been researched along with Brown Tendon Sheath Syndrome in 9 studies
Apnea: A transient absence of spontaneous respiration.
| Excerpt | Relevance | Reference |
|---|---|---|
| " A comparison of central nervous system signs in syndromic vs nonsyndromic mitochondrial diseases revealed significant differences in terms of headache, external ocular motility, and apnea (P < 0." | 3.76 | Clinical manifestations in children with mitochondrial diseases. ( Chen, LH; Chi, CS; Lee, HF; Lee, HJ; Tsai, CR, 2010) |
| ", apnea, neurogenic dysphagia [ND], gastro-esophageal reflux disease [GERD], neuro-ophthalmologic disturbances [NOD])." | 3.74 | Reversal of hindbrain herniation after maternal-fetal surgery for myelomeningocele subsequently impacts on brain stem function. ( Adzick, NS; Bebbington, MW; Danzer, E; Finkel, RS; Johnson, MP; Rintoul, NE; Schwartz, ES; Zarnow, DM, 2008) |
| "We review the anesthetic implications of Joubert syndrome and report that spinal anesthesia under intravenous propofol sedation proved satisfactory for repair of an inguinal hernia in a spontaneously ventilating infant with this syndrome." | 3.72 | Anesthetic management in Joubert syndrome. ( Gordon, GJ; Vodopich, DJ, 2004) |
| " He had episodic tachypnea and apnea, inspiratory stridor, aspiration, and growth and mental retardation." | 3.71 | Bifid epiglottis associated with Joubert's syndrome. ( Kim, JW; Kim, KH; Sung, MW, 2001) |
| " The clinical presentations included panting respiration with apnea in the newborn period (4/4), psychomotor retardation (4/4) and ataxia (2/4)." | 3.68 | Joubert syndrome in Chinese infants and children: a report of four cases. ( Chen, CH; Chi, CS; Mak, SC; Shian, WJ, 1993) |
| "It is characterized by infantile seizures refractory to anticonvulsive treatments, microcephaly, delays in mental and motor development, spasticity, ataxia, dysarthria and other paroxysmal neurologic phenomena, often occurring prior to meals." | 2.44 | [Glucose transporter type 1 (GLUT-1) deficiency]. ( Cano, A; Chabrol, B; Ticus, I, 2008) |
| "Joubert syndrome is a rare and probably underdiagnosed syndrome with bad prognosis." | 1.30 | [Joubert syndrome: a report of 5 cases]. ( Calleja-Pérez, B; Fernández-Jaén, A; Martínez-Bermejo, A; Pascual-Castroviejo, I, 1998) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 2 (22.22) | 18.2507 |
| 2000's | 6 (66.67) | 29.6817 |
| 2010's | 1 (11.11) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Cano, A | 1 |
| Ticus, I | 1 |
| Chabrol, B | 1 |
| Danzer, E | 1 |
| Finkel, RS | 1 |
| Rintoul, NE | 1 |
| Bebbington, MW | 1 |
| Schwartz, ES | 1 |
| Zarnow, DM | 1 |
| Adzick, NS | 1 |
| Johnson, MP | 1 |
| Chi, CS | 2 |
| Lee, HF | 1 |
| Tsai, CR | 1 |
| Lee, HJ | 1 |
| Chen, LH | 1 |
| Vodopich, DJ | 1 |
| Gordon, GJ | 1 |
| Utsch, B | 1 |
| Sayer, JA | 1 |
| Attanasio, M | 1 |
| Pereira, RR | 1 |
| Eccles, M | 1 |
| Hennies, HC | 1 |
| Otto, EA | 1 |
| Hildebrandt, F | 1 |
| Shian, WJ | 1 |
| Mak, SC | 1 |
| Chen, CH | 1 |
| Calleja-Pérez, B | 1 |
| Fernández-Jaén, A | 1 |
| Martínez-Bermejo, A | 1 |
| Pascual-Castroviejo, I | 1 |
| Sung, MW | 1 |
| Kim, JW | 1 |
| Kim, KH | 1 |
| Zamponi, N | 1 |
| Rossi, B | 1 |
| Messori, A | 1 |
| Polonara, G | 1 |
| Regnicolo, L | 1 |
| Cardinali, C | 1 |
1 review available for apnea and Brown Tendon Sheath Syndrome
| Article | Year |
|---|---|
[Glucose transporter type 1 (GLUT-1) deficiency].
Topics: Aging; Apnea; Blood-Brain Barrier; Brain Diseases; Developmental Disabilities; Glucose Transporter T | 2008 |
8 other studies available for apnea and Brown Tendon Sheath Syndrome
| Article | Year |
|---|---|
Reversal of hindbrain herniation after maternal-fetal surgery for myelomeningocele subsequently impacts on brain stem function.
Topics: Apnea; Arnold-Chiari Malformation; Brain Stem; Child; Child, Preschool; Decompression, Surgical; Deg | 2008 |
Clinical manifestations in children with mitochondrial diseases.
Topics: Administration, Oral; Adolescent; Apnea; Cardiovascular Diseases; Child; Child, Preschool; Female; G | 2010 |
Anesthetic management in Joubert syndrome.
Topics: Agenesis of Corpus Callosum; Anesthesia; Anesthesia, Caudal; Apnea; Ataxia; Brain; Corpus Callosum; | 2004 |
Identification of the first AHI1 gene mutations in nephronophthisis-associated Joubert syndrome.
Topics: Adaptor Proteins, Signal Transducing; Adaptor Proteins, Vesicular Transport; Adolescent; Adult; Apne | 2006 |
Joubert syndrome in Chinese infants and children: a report of four cases.
Topics: Apnea; Ataxia; Brain; Child, Preschool; Female; Humans; Infant; Male; Ocular Motility Disorders; Psy | 1993 |
[Joubert syndrome: a report of 5 cases].
Topics: Apnea; Ataxia; Brain; Chromosome Aberrations; Chromosome Disorders; Female; Humans; Infant; Infant, | 1998 |
Bifid epiglottis associated with Joubert's syndrome.
Topics: Abnormalities, Multiple; Apnea; Cerebellum; Child, Preschool; Epiglottis; Humans; Intellectual Disab | 2001 |
Joubert syndrome with associated corpus callosum agenesis.
Topics: Agenesis of Corpus Callosum; Apnea; Cerebellum; Female; Humans; Infant; Magnetic Resonance Imaging; | 2002 |