1. Brainstem stroke syndromes, also known as crossed Brainstem syndromes, refer to a group of syndromes that occur secondary to lesions, most commonly infarcts, of the Brainstem

2. Epidemiology Although many different Brainstem stroke syndromes have

3. Complete apallic syndromes differ from incomplete similar syndromes which show remnants of telencephalic functions (severe dementia, global agnosia, etc.), including an abnormal EEG.

4. Benzene exposure is associated with myelodysplastic syndromes

5. Manifestations of somnolence, stupor, coma, confusion, decorticated syndromes .

6. An elevated risk of WT is also observed in some overgrowth syndromes, various tumor predisposition syndromes, and specific constitutional aneuploidies.

7. Generating crc syndromes with data extracted from syndrome loop

8. Pulmonary hemorrhagic syndromes and alveolar proteinosis may be diagnosed unequivocally.

9. Start studying Nephritic and Nephrotic Syndromes, Renal Tubular Acidoses

10. Two syndromes in particular are associated with esophageal Atresia:

11. Have you yourself experienced any of the syndromes you write about?

12. Chromosomal deletion syndromes result from loss of parts of Chromosomes

13. The diagnosis and genesis of the syndromes are discussed with the literature.

14. 12 Pulmonary embolism ( PE ) is one of the common clinical pathological syndromes.

15. L L and S 1 nerve root syndromes are typical in sciatica.

16. The term “peripheral neuropathic pain syndromes” summarizes several chronic pain syndromes, which can occur focally or generalized in the peripheral nervous system in the course of an impairment of afferent neurons.

17. There is no set common convention for the naming of newly identified syndromes.

18. We regard diffusion-weighted MRI as a powerful means to differentiate acute amnestic syndromes.

19. Ampullary Adenomas occur sporadically and in the setting of familial polyposis syndromes

20. Chronic muscular skeletal pain syndromes (CMSPS) are one of the major health issues.

21. Objective: To explore the rule of quantitative diagnosis of syndromes in apoplectic sequela.

22. Method for maximising the correction capability of an error-correcting code, using additional syndromes

23. Little is known about the type and frequency of psycho-organic syndromes among prisoners.

24. Earlobe Creases have been found to be a sign of some rare genetic syndromes

25. Electrophysiologic testing is an essential part of the evaluation of Anterior interosseous nerve syndromes.

26. These Clefts are present in various syndromes, but can also occur unrelated to a syndrome.

27. The differential diagnosis of psychogenic vs. organic amnestic syndromes may cause difficulty in certain cases.

28. Methods Study the interrelationship of syndromes through the measurement and content of gasticmucosa growth inhibition change.

29. Withdrawal syndromes: unrecognized or improperly managed. Interactions of abused drugs with anaesthetics and adjunctive drugs.

30. The existence of these genetic syndromes brings forth . the fact that aging is a genetic phenomenon .

31. The differentiation between degenerative syndromes of the cervical spine and post-traumatic symptoms requires accident analysis.

32. Craniofacial anomalies associated with congenital syndromes such as 22q11.2 deletion, Apert, Pfieffer or Treacher-Collins.

33. Both syndromes are characterized by a high prevalence and a severely disturbed quality of life.

34. This disease is generally associated with elevated secretion of Androgens, sometimes resulting in virilizing syndromes, including genital ambiguity, precocious puberty in both sexes, or milder syndromes of androgen excess like precocious pubarche or the occurrence of …

35. However, they occur more frequently when adjacent organs or structures are involved, thus creating very complex syndromes.

36. Bove and colleagues (2018) stated that there is no consensus on criteria for Accelerometric diagnosis of tremor syndromes

37. They would eventually learn to recognize such syndromes in families, track down the faulty genes and devise interventions.

38. Achondroplasias Dysplasia, SADDAN Dysplasias, SADDAN SADDAN SADDAN Dysplasia SADDAN Dysplasias SADDANs Severe Achondroplasia with Developmental Delay and Acanthosis Nigricans Skeleton Skin Brain Syndrome Skeleton-Skin-Brain Syndrome Skeleton-Skin-Brain Syndromes Syndrome, Skeleton-Skin-Brain Syndromes, Skeleton-Skin-Brain

39. Clinical picture compatible with Chlamydia trachomatis infection, e.g. urethritis, epididymitis, cervicitis, acute salpingitis or other syndromes when sexually transmitted.

40. Ainhum and PseudoAinhum Are Syndromes Related to External Constricting Bands; Constricting bands are classified as Ainhum and pseudoAinhum

41. The possibilities and limitations of molecular genetic studies can be illustrated by the example of androgen insensitivity syndromes.

42. The Most Advanced Treatments: Thanks to advances in treatment, many children with Craniofacial syndromes can achieve a happy life

43. Objective: Cannabidiol is efficacious as an adjunctive treatment in children with epilepsy associated with Dravet and Lennox-Gastaut syndromes

44. Discussion: In conclusion, Reye-like syndromes and dicarboxylic aciduria in infancy may be the first signs of cystic fibrosis.

45. Bartter and Gitelman syndromes are both autosomal recessive conditions characterized by renal salt wasting, hypokalemia, and metabolic alkalosis.

46. The clinical features of Pterygoarthromyodysplasia congenita are described and differentiated from those of other syndromes with pyterygium formation.

47. Andrology is the medical specialty that deals with male health, particularly related to male reproductive system and urological syndromes

48. Clinical picture compatible with Chlamydia trachomatis infection, e.g. urethritis, epididymitis, cervicitis, acute salpingitis or other syndromes when sexually transmitted

49. Bilobed Structure: Disease Bioinformatics Research of Bilobed Structure has been linked to Nervousness, Stomatitis, Biliary Obstruction, Immunologic Deficiency Syndromes, Fibrosis

50. Activities i. Establish the means for early, systematic evaluation of newly recognized pathogens or syndromes of probable infectious etiology.

51. Schematically, three clinical syndromes with increasing severity are described: breathing with the mouth open, snoring and sleep Apneal hypopnea syndrome

52. These crystals are responsible for different rheumatic syndromes, including acute or chronic synovial inflammation, and also contribute to cartilage degeneration.

53. A total of 179 adrenalectomies have been performed in patients with endocrine-secreting tumours (pheochromocytomas). Conn and Cushing syndromes are presented.

54. Aphthae is a clinical diagnosis that should be included in the differential of genital ulcers in the setting of febrile syndromes

55. Both syndromes indicate an increased risk for subsequent somatic morbidity, worsening depression functional deterioration, admission to a nursing home and mortality.

56. 19 Conclusion Continuous blood purification is one of effective treatments for Senility seriously hemorrhagic fever with renal syndromes and be batt...

57. The DSM-5 recategorizes Adjustment disorders as a “heterogeneous array of stress response syndromes that occur after exposure to a distressing (traumatic or nontraumatic

58. Bartter Syndromes are inherited disorders of the kidney that cause salts and water to be lost from the body in the urine

59. Specific clinical applications will include migraine and headache aphasias, agnosias, perceptual disorders, neglect syndromes, dementias (including organic brain syndrome) and developmental disorders.

60. Not only can Ascarids and hookworms cause disease in their respective hosts, they are also well-known causes of larva migrans syndromes in …

61. Bartter Syndromes are inherited disorders of the kidney that cause salts and water to be lost from the body in the urine

62. Frontal Bossing is present when the forehead is very prominent with depression of the nasal bridge, and has been described in a number of syndromes

63. From a neurobiological perspective, three syndromes emerge that relate to specific dysfunctions of afferent cholinergic and serotonergic visual circuitry and promise future therapeutic advances.

64. Disorders of energy metabolism and “endogenous intoxications” (syndromes leading to hyperammonemia, hyperhomocysteinemia, porphyria, aminoacidopathy, and organic aciduria) represent the two major categories of IEMs.

65. A complete family and personal history, physical examination, and neuroimaging, as well as comprehensive laboratory evaluation may be required for the diagnosis of Ataxic syndromes

66. Biotherapy is defined as the therapy of hormonal hypersecretion syndromes and/or tumor growth with substances, or pharmacological derivatives thereof, occurring naturally in the body

67. Distraction is indicated in hemifacial microsomias, multiple syndromes with mandibular malformations, mandibular retrognathia, posttraumatic jaw deficiencies, craniofacial malformations, alveolar ridge resorptions, and alveolar ridge resections.

68. But the majority of Anti- Convulsant Drugs (AED’s), around 10 of which, includes the newer drugs, that may cause the condition Foetal AntiConvulsant Syndromes in various degrees

69. Anterolateral ankle impingement is one of the impingement syndromes of the ankle and can occur as a posttraumatic sequel of an inversion injury 1-6.

70. Leading symptom is primary, hypergonadotropic amenorrhea with normal body height and usually without associated anomalies, with the exception of the Turner syndrome and other rare syndromes.

71. The absence of significant stenosis on coronary angiography and spontaneous improvement of ventricular akinesia are very important features that distinguish this syndrome from acute coronary syndromes.

72. Advantageous Predictors of Acute Coronary Syndromes Evaluation (Apace) Study (Apace) The safety and scientific validity of this study is the responsibility of the study sponsor and investigators

73. The common basis for hemophagocytic syndromes are genetic or acquired immune defects which lead to an exaggerated but ineffective immune response with high levels of inflammatory cytokines.

74. Bartter and Gitelman syndromes are renal tubular salt-wasting disorders in which the kidneys cannot reabsorb chloride in the TALH or the DCT, depending on the mutation

75. Such results raise the possibility that the RES plays a pivotal role in the circulatory manifestations of compound 48/80 and anaphylactic-type (histamine release) shock syndromes.

76. Megestrol Acetate (MGA), sold under the brand name Megace among others, is a progestin medication which is used mainly as an appetite stimulant to treat wasting syndromes such as cachexia

77. The importance of the EEG for the clinical diagnostics of Alzheimer’s disease and acute delirium as well as the differentiation between psychiatric syndromes and non-convulsive status epilepticus is reviewed.

78. In some cases neuroplastic changes in the spinal dorsal horn and sympathetic-afferent coupling play a role in the development of chronic pain syndromes and complicate the treatment.

79. From a total of 51 adenomas 17 prolactinomas (33.3%), 15 Acromegalies (29.4%), 4 Cushing-syndromes (7.8%), 1 TSH-producing adenoma (1.9%) and 14 hormone-inactive adenomas (27.4%) were found

80. This article reviews the current evidence on the natural history of aortic arch aneurysms and acute aortic syndromes, including penetrating ulcers, intramural hematomas, acute and chronic type B dissections.