- Diagnnosis and Treatment of the Comatous Patient
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No authors listed
- KMID: 1663658
- J Korean Pediatr Soc.
- 1978 Aug;21(8):640-643.
No abstract available. -
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- A Case of Apert syndrome(Acrocephaosyndactyly)
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Chang IS, Yang DK, Kim KB
- KMID: 1663647
- J Korean Pediatr Soc.
- 1978 Aug;21(8):605-610.
Apert syndrome is a rare disorder characterized by malformation of the skull, (usually oxyce-phaly or acrocephaly), in association with sys temic syndactyly It is due to congenital disturbance in the... -
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- A Case of Male Turner Syndrome
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Kim KB, Yang DK, Yoon YS
- KMID: 1663649
- J Korean Pediatr Soc.
- 1978 Aug;21(8):611-616.
We prsent here a 6 year old who has abnormalities of his genitalia, as well as other characteristic features typical of Turner syndrome. He has a small penis with hypospadias,... -
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- A Case of Prune-Belly Syndromes
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Kim DK, Choi BH, Yim CJ, Kim SK
- KMID: 1663651
- J Korean Pediatr Soc.
- 1978 Aug;21(8):617-622.
We have recently experienced a case of prune-belly syndrome, in 119/12-year-old male child with congenital defects of abdominal muscles, cryptorchidism, hydronephrosis, megacystis and spina bifida. Diagnosis was confirmed by EMG,... -
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- Ketogenic Diet Trial for The Treatment of Minor Motor Seizures
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Suck SP, Lee JG, Kem SH, Choe HW
- KMID: 1663641
- J Korean Pediatr Soc.
- 1978 Aug;21(8):579-586.
A 3-years-old girl, diagnosed as infantile spasm and 5-years-old boy, diagnosed as akinetic seizure were subjected to ketogenic diet trial because of their poor responses anticonyulsant treatment After adding ketogenic... -
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- Clinical Evaluation of Postnatal Weight Gain in Premature and Low Birth Weight Infants
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Kim HK
- KMID: 1663643
- J Korean Pediatr Soc.
- 1978 Aug;21(8):587-594.
Among premature and low birth weight infants admitted between March 1970 and February 1977, 228 infants who were clinically normal and older than 7 hospital days are evaluated as to... -
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- A Case of Aeute Werdnig-Hoffmann Disease
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Song YM, Lee KS, Shin JJ, Kang SC, Ji JK
- KMID: 1663653
- J Korean Pediatr Soc.
- 1978 Aug;21(8):623-629.
Acute Werdnig-Hoffmann disease is genetically determined progressive degenerative disease of anterior spinal neuron, characterized by fasciculations of the tongue usually occuring along with flaccid paralysis of extremities with intact mentality.... -
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- A Case Report of the Idiopathic Hypoparathyroidism with Tridione Induced Nephrotic Syndrome
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Lee DH, Chang HJ, Lee HJ, Ko KW
- KMID: 1663656
- J Korean Pediatr Soc.
- 1978 Aug;21(8):630-636.
A case of idiopathic hypoparathyroidism with tridione induced nephrotic syndrome is presented with a brief review of literature. He had been suffered from hypocalcemic tetany symptoms due to didopathic hypoparathyroidism... -
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- Clinical Observation of Diphtheria
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Lee CU, Moon HK, Shin JW
- KMID: 1663645
- J Korean Pediatr Soc.
- 1978 Aug;21(8):595-604.
We have observed clinically 57 cases of diphtheria, admitted to Dept. of Pediatrics and E. N. T. of College of Medicine, Busan National University during a period of past 4... -
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