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Search Results - El‐Darouti, Mohamed
Search Results - El‐Darouti, Mohamed
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A homozygous mutation in RNU4ATAC as a cause of microcephalic osteodysplastic primordial dwarfism type I (MOPD I) with associated pigmentary disorder
by
Abdel‐Salam, Ghada M.H.
,
Miyake, Noriko
,
Eid, Maha M.
,
Abdel‐Hamid, Mohamed S.
,
Hassan, Nihal A.
,
Eid, Ola M.
,
Effat, Laila K.
,
El‐Badry, Tarek H.
,
El‐Kamah, Ghada Y.
,
El‐Darouti, Mohamed
,
Matsumoto, Naomichi
Published in
American journal of medical genetics. Part A
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Pentoxifylline (Anti-Tumor Necrosis Factor Drug): Effective Adjuvant Therapy in the Control of Ocular Cicatricial Pemphigoid
by
Darouti, Mohamed A. El
,
Khattab, Mohamed A. Fakhry
,
Hegazy, Rehab A.
,
Hafez, Dalia A.
,
Gawdat, Heba I.
Published in
European journal of ophthalmology
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Ligneous Conjunctivitis with Oral Mucous Membrane Involvement and Decreased Plasminogen Level
by
El‐Darouti, Mohamed
,
Zayed, Amira A.
,
El‐Kamah, Ghada Y.
,
Mostafa, Mostafa I.
Published in
Pediatric dermatology
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Impetigo herpetiformis during the puerperium triggered by secondary hypoparathyroidism: a case report
by
Fouda, Usama M
,
Fouda, Ragai M
,
Ammar, Hussam M
,
Salem, Mohamed
,
Darouti, Mohamed El
Published in
Cases journal
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A novel frameshift mutation of COL7A1 in an Egyptian patient with autosomal recessive dystrophic epidermolysis bullosa
by
El-Kamah, Ghada
,
Mansour, Lamia
,
Mahmoud, Enas
,
El Darouti, Mohamed
,
Radwan, Hoda
,
Amr, Khalda
Published in
Middle East Journal of Medical Genetics
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Sulfasalazine and pentoxifylline in psoriasis: A possible safe alternative
by
El-Mofty, Medhat
,
El-Darouti, Mohamed
,
Rasheed, Hoda
,
Bassiouny, Dalia Ahmed
,
Abdel-Halim, Mona
,
Zaki, Naglaa Sameh
,
El-Hanafy, Ghada
,
El-Hadidi, Heba
,
Azzam, Omar
,
El-Ramly, Amany
,
Fawzy, Marwa
Published in
The Journal of dermatological treatment
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Ligneous Conjunctivitis with Oral Mucous Membrane Involvement and Decreased Plasminogen Level
by
El-Darouti, Mohamed
,
Zayed, Amira A.
,
El-Kamah, Ghada Y.
,
Mostafa, Mostafa I.
Published in
Pediatric Dermatology
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A homozygous mutation in RNU4ATAC as a cause of microcephalic osteodysplastic primordial dwarfism type I (MOPD I) with associated pigmentary disorder
by
Abdel-Salam, Ghada M.H.
,
Miyake, Noriko
,
Eid, Maha M.
,
Abdel-Hamid, Mohamed S.
,
Hassan, Nihal A.
,
Eid, Ola M.
,
Effat, Laila K.
,
El-Badry, Tarek H.
,
El-Kamah, Ghada Y.
,
El-Darouti, Mohamed
,
Matsumoto, Naomichi
Published in
American Journal of Medical Genetics Part A
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Scleromyxedema: A novel therapeutic approach
by
El-Darouti, Mohammad Ali, MD
,
Hegazy, Rehab Aly, MD
,
Fawzy, Marwa Mohamed, MD
,
Mahmoud, Sara Bahaa, MD
,
Dorgham, Dina Ahmed, MSc
Published in
Journal of the American Academy of Dermatology
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American Journal Of Medical Genetics. Part A
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Conjunctiva - Pathology
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Drug Therapy, Combination
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Fair Skin
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Hypogenesis Of Corpus Callosum
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Microcephalic Osteodysplastic Primordial Dwarfism I
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