scholarly journals VP24.06: Unilateral microphthalmia and CNS‐associated anomalies: management and prognosis

2021 ◽  
Vol 58 (S1) ◽  
pp. 201-201
Author(s):  
R. Radulescu‐Botica
Keyword(s):  
2010 ◽  
Vol 14 (1) ◽  
pp. 42 ◽  
Author(s):  
Joo Whee Kim ◽  
Se Eun Lee ◽  
Yun Hye Jung ◽  
Kyung Hee Han ◽  
Hyun Kyung Lee ◽  
...  

1992 ◽  
Vol 28 (1) ◽  
pp. 156
Author(s):  
Hyeon Kyeong Lee ◽  
Kyung Mo Yeon ◽  
Young Hi Choe ◽  
In One Kim ◽  
Yun Hyun Choe ◽  
...  

1974 ◽  
Vol 23 (S1) ◽  
pp. 345-347
Author(s):  
F. Mollica ◽  
L. Pavone ◽  
Harvey L. Levy

Type II hyperprolinemia is a rare metabolic disorder associated with mental retardation, seizures, and EEG anomalies.The authors describe a Sicilian family, detected screening for aminoacidopathies by the method of Scriver, in which three siblings have high levels of serum proline and urinary pyrroline-5-carboxylic acid, without any signs of associated anomalies.


2021 ◽  
Vol 224 (2) ◽  
pp. S175
Author(s):  
Jennifer E. Powel ◽  
Michail Spiliopoulos ◽  
Carlos R. Ferreira ◽  
Emily Rosenthal ◽  
Elena Sinkovskaya ◽  
...  

2021 ◽  
Author(s):  
C Caldeman ◽  
A Fogelström ◽  
J Oddsberg ◽  
C Mesas Burgos ◽  
A Löf Granström

2001 ◽  
Vol 9 (3) ◽  
pp. 232-233
Author(s):  
Harinder Singh Bedi ◽  
Maninder Singh Kalkat ◽  
Ved Prakash Sharma ◽  
Vijay Mahajan
Keyword(s):  

1999 ◽  
Vol 1 (4) ◽  
pp. 29-29
Author(s):  
L. R. Shapiro
Keyword(s):  

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