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Adnan Yuksel

Showing results (11-20 of 32) with videos related to

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Headache|January 16, 2008
Spontaneous intracranial hypotension syndrome in a patient with marfan syndrome and autosomal dominant polycystic kidney diseaseSait Albayram, Ahmet Baş, Harun Ozer, et al.
Molecular Syndromology|May 13, 2026
<i>CHAMP1</i>-Related Neurodevelopmental Disorder: Two Turkish Cases with Novel Truncating Variants and Literature ReviewZehra Manav Yigit, Pelin Ozyavuz Cubuk, Kamil Utku Bayrak, et al.
Clinical Dysmorphology|February 2, 2002
Neuroblastoma in a dysmorphic girl with a partial duplication of 2p caused by an unbalanced translocationAdnan Yuksel, Mehmet Seven, Birsen Karaman, et al.
Molecular Biology Reports|May 8, 2013
MicroRNA profiling in lymphocytes and serum of tyrosinemia type-I patientsOmer Faruk Karatas, Esra Guzel, Ender Karaca, et al.
Pediatric Neurology|March 18, 2014
Therapeutic plasma exchange for malignant refractory status epilepticus: a case reportAhmet H Gedik, Demet Demirkol, Burak Tatlı, et al.
Gene|July 13, 2013
A novel EFNB1 mutation in a patient with craniofrontonasal syndrome and right hallux duplicationMehmet Seven, Alper Gezdirici, Hakan Ulucan, et al.
Clinical Dysmorphology|November 22, 2012
A rare case of split hand/foot malformation with sensorineural hearing loss and Mondini dysplasiaAlper Gezdirici, Alper Yenigun, Erkan Koparir, et al.
Drug and Chemical Toxicology|November 1, 2013
Melatonin attenuates phenytoin sodium-induced DNA damageUfuk Erenberk, Rusen Dundaroz, Ozlem Gok, et al.
American Journal of Medical Genetics. Part A|July 22, 2014
Poikiloderma with neutropenia: genotype-ethnic origin correlation, expanding phenotype and literature reviewAsuman Koparir, Alper Gezdirici, Erkan Koparir, et al.
Clinical Dysmorphology|January 18, 2013
Circumferential skin folds and multiple anomalies: confirmation of a distinct autosomal recessive Michelin tire baby syndromeHakan Ulucan, Erkan Koparir, Asuman Koparir, et al.
Pageof 4

Showing results (11-20 of 32) with videos related to

Sort By:
Pageof 4
Headache|January 16, 2008
Spontaneous intracranial hypotension syndrome in a patient with marfan syndrome and autosomal dominant polycystic kidney diseaseSait Albayram, Ahmet Baş, Harun Ozer, et al.
Molecular Syndromology|May 13, 2026
<i>CHAMP1</i>-Related Neurodevelopmental Disorder: Two Turkish Cases with Novel Truncating Variants and Literature ReviewZehra Manav Yigit, Pelin Ozyavuz Cubuk, Kamil Utku Bayrak, et al.
Clinical Dysmorphology|February 2, 2002
Neuroblastoma in a dysmorphic girl with a partial duplication of 2p caused by an unbalanced translocationAdnan Yuksel, Mehmet Seven, Birsen Karaman, et al.
Molecular Biology Reports|May 8, 2013
MicroRNA profiling in lymphocytes and serum of tyrosinemia type-I patientsOmer Faruk Karatas, Esra Guzel, Ender Karaca, et al.
Pediatric Neurology|March 18, 2014
Therapeutic plasma exchange for malignant refractory status epilepticus: a case reportAhmet H Gedik, Demet Demirkol, Burak Tatlı, et al.
Gene|July 13, 2013
A novel EFNB1 mutation in a patient with craniofrontonasal syndrome and right hallux duplicationMehmet Seven, Alper Gezdirici, Hakan Ulucan, et al.
Clinical Dysmorphology|November 22, 2012
A rare case of split hand/foot malformation with sensorineural hearing loss and Mondini dysplasiaAlper Gezdirici, Alper Yenigun, Erkan Koparir, et al.
Drug and Chemical Toxicology|November 1, 2013
Melatonin attenuates phenytoin sodium-induced DNA damageUfuk Erenberk, Rusen Dundaroz, Ozlem Gok, et al.
American Journal of Medical Genetics. Part A|July 22, 2014
Poikiloderma with neutropenia: genotype-ethnic origin correlation, expanding phenotype and literature reviewAsuman Koparir, Alper Gezdirici, Erkan Koparir, et al.
Clinical Dysmorphology|January 18, 2013
Circumferential skin folds and multiple anomalies: confirmation of a distinct autosomal recessive Michelin tire baby syndromeHakan Ulucan, Erkan Koparir, Asuman Koparir, et al.
Pageof 4