MYOPATHIA DISTALIS TARDA HEREDITARIA (WELANDERS SYNDROME)REPORT OF A CASE

被引：0

|

作者：

VILLANUE.GR

机构：

来源：

ELECTROENCEPHALOGRAPHY AND CLINICAL NEUROPHYSIOLOGY | 1968年 / 24卷 / 04期

关键词：

D O I：

暂无

中图分类号：

R318 [生物医学工程];

学科分类号：

0831 ;

摘要：

引用

收藏

页码：388 / &

相关论文

共 50 条

[41] EPIDERMOLYSIS BULLOSA HEREDITARIA - REPORT OF A CASE WITH UNUSUAL ASSOCIATED DEFORMITIES
KITLOWSKI, EA
BANFIELD, EE
[J]. PLASTIC AND RECONSTRUCTIVE SURGERY, 1948, 3 (04) : 481 - 488
[42] Olmesartan medoxomilFirst report of porphyria cutanea tarda: case report
[J]. Reactions Weekly, 2010, 1315 (1) : 37 - 37
[43] Myonecrosis caused by Edwardsiella tarda:: A case report and case series of extraintestinal E. tarda infections
Slaven, EM
Lopez, FA
Hart, SM
Sanders, CV
[J]. CLINICAL INFECTIOUS DISEASES, 2001, 32 (10) : 1430 - 1433
[44] Tipranavir/ritonavirFirst report of porphyria cutanea tarda: case report
[J]. Reactions Weekly, 2007, 1162 (1) : 25 - 25
[45] EPIDERMOLYSIS BULLOSA HEREDITARIA LETALIS - REPORT OF A CASE AND PROBABLE ULTRASTRUCTURAL DEFECTS
HASHIMOTO, I
ANTONLAMPRECHT, I
MEYBURG, P
[J]. HELVETICA PAEDIATRICA ACTA, 1976, 30 (06) : 543 - 552
[46] KERATOMA HEREDITARIA MUTILANS - REPORT OF A CASE WITH SUCCESSFUL SURGICAL-TREATMENT
LUK, KDK
WU, PC
CHOW, SP
[J]. JOURNAL OF HAND SURGERY-AMERICAN VOLUME, 1986, 11A (02): : 269 - 272
[47] Sporadic Dyschromatosis Universalis Hereditaria: A Second Case Report From Iran
Dogohar, Sasan
Alirezaei, Pedram
Basir, Hamidreza Ghasemi
Jamshidi, Mohammad
Etaee, Farshid
[J]. CUREUS JOURNAL OF MEDICAL SCIENCE, 2021, 13 (07)
[48] PravastatinPorphyria cutanea tarda in an elderly patient: case report
[J]. Reactions Weekly, 1998, 731 (1) : 10 - 10
[49] Scleral Necrosis in Porphyria Cutanea Tarda: A Case Report
Shukla, Ruchi
Mishra, Ashutosh Kumar
Pandey, Prasoon
[J]. JOURNAL OF CLINICAL AND DIAGNOSTIC RESEARCH, 2022, 16 (02) : 1 - 3
[50] Busulfan/cyclophosphamide/melphalanPorphyria cutanea tarda: case report
[J]. Reactions Weekly, 2018, 1729 (1) : 57 - 57

← 1 2 3 4 5 →